Replikin peptides in rapid replication of glioma cells and in influenza epidemics

ABSTRACT

Peptides of influenza virus hemagglutinin protein and  Plasmodium falciparum  malaria antigen, antibodies specific for the peptides, influenza vaccines, malaria vaccines and methods of stimulating the immune response of a subject to produce antibodies to influenza virus or malaria are disclosed. Also disclosed are methods for formulating vaccines for influenza virus.

CROSS REFERENCE TO OTHER APPLICATIONS

This application is a Continuation-In-Part Application of U.S. Ser. No. 09/984,057, filed Nov. 26, 2001, which claims priority from Provisional Application 60/303,396, filed Jul. 9, 2001 and Provisional Application U.S. 60/278,761 filed Mar. 27, 2001, the subject matter of which is incorporated by reference hereto.

FIELD OF THE INVENTION

This invention relates to the identification and use of Replikins, a class of peptides that share structural characteristics. In particular, this invention relates to Replikins which have been identified in influenza viruses and their use in designing influenza virus vaccines.

BACKGROUND OF THE INVENTION

Influenza is an acute respiratory illness of global importance. Despite international attempts-to control influenza virus-outbreaks through vaccination influenza infections remain an important cause of morbidity and mortality. Worldwide influenza pandemics have occurred at irregular and previously unpredictable intervals throughout history and it is expected that they will continue to occur in the future. The impact of pandemic influenza is substantial in terms of morbidity, mortality and economic cost.

Influenza vaccines remain the most effective defense against influenza virus, but because of the ability of the virus to mutate and the availability of non-human host reservoirs it is expected that influenza will remain an emergent or re-emergent infection. Global influenza surveillance indicates that influenza viruses may vary within a country and between countries and continents during an influenza season. Virologic surveillance is of importance in monitoring antigenic shift and drift. Disease surveillance is also important in assessing the impact of epidemics. Both types of information have provided the basis of vaccine composition and the correct use of antivirals. However, to date there has been only annual post hoc hematological classification of the increasing number of emerging influenza virus strains, and no specific chemical structure of the viruses has been identified as an indicator of approaching influenza epidemic or pandemic. Currently, the only basis for annual classification of influenza virus as active, inactive or prevalent in a given year is the activities of the virus hemagglutinin and neuraminidase proteins. No influenza viral chemical structure has been identified that can be used for quantitative warning of epidemics or pandemics or to design more effective and safer vaccines.

Because of the annual administration of influenza vaccines and the short period of time when a vaccine can be administered, strategies directed at improving vaccine coverage are of critical importance.

Another disease which has proved difficult to treat and for which there is no effective vaccine is malaria. Malaria causes much physical and economic hardship in tropical regions. Malaria is caused by Plasmodzium falciparum, which has proved to be extremely resistant to treatment and to date, a vaccine for malaria remains elusive. Thus, there is a need for effective malaria vaccines and methods of treating or preventing the disease.

SUMMARY OF THE INVENTION

In one aspect of the invention there are provided isolated influenza virus peptides containing a Replikin sequence. The influenza virus peptides comprise from 7 to about 50 amino acids including (1) at least one lysine residue located six to ten amino acid residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.

In another aspect of the invention there is provided a process for stimulating the immune system of a subject to produce antibodies that bind specifically to an influenza virus Replikin sequence, said process comprising administering to the subject an effective amount of a dosage of a composition comprising at least one influenza virus replikin peptide. In a preferred embodiment the composition comprises at least one peptide that is present in an emerging strain of influenza virus.

The present invention also provides antibodies that bind specifically to an influenza virus Replikin, as defined herein, as well as antibody cocktails containing a plurality of antibodies that specifically bind to influenza virus Replikins. In one embodiment of the invention, there are provided compositions comprising an antibody or antibodies that specifically bind to an influenza Replica and a pharmaceutically acceptable carrier.

The present invention also provides therapeutic compositions comprising one or more of isolated influenza virus peptides having from 7 to about 50 amino acids comprising

1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues, and a pharmaceutically acceptable carrier.

In another aspect of the invention there is provided an antisense nucleic acid molecule complementary to an influenza virus hemagglutinin Replikin mRNA sequence, said Replikin mRNA sequence having from 7 to about 50 amino acids comprising

(1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.

In yet another aspect of the invention, there is provided a method of stimulating the immune system of a subject to produce antibodies to influenza virus comprising administering an effective amount of at least one influenza virus Replikin peptide having from 7 to about 50 amino acids comprising (1) at least one lysine residue located six to ten amino acid residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.

In another aspect, there is provided a method of selecting an influenza virus peptide for inclusion in an influenza virus vaccine comprising

(1) obtaining at least one isolate of each strain of a plurality of strains of influenza virus,

(2) analyzing the hemagglutinin amino acid sequence of the at least one isolate of each strain of the plurality of strains of influenza virus for the presence and concentration of Replikin sequences,

(3) comparing the concentration of Replikin sequences in the hemagglutinin amino acid sequence of the at least one isolate of each strain of the plurality of strains of influenza virus to the concentration of Replikin sequences observed in the hemagglutinin amino acid sequence of each of the strains at at least one earlier time period to provide the concentration of Replikins for at least two time periods, said at least one earlier time period being within about six months to about three years prior to step (1),

(4) identifying the strain of influenza virus having the highest increase in concentration of Replikin sequences during the at least two time periods,

(5) selecting at least one Replikin sequence present in the strain of influenza virus peptide identified in step (4) as a peptide for inclusion in an influenza virus vaccine.

The present invention also provides a method of making an influenza virus vaccine comprising

(1) identifying a strain of influenza virus as an emerging strain,

(2) selecting at least one Replikin sequence present in the emerging strain as a peptide template for influenza virus vaccine manufacture,

(3) synthesizing peptides having the amino acid sequence of the at least one Replikin sequence selected in step (2), and

(4) combining a therapeutically effective amount of the peptides of step (4) with a pharmaceutically acceptable carrier and/or adjuvant.

In another aspect, the invention is directed to a method of identifying an emerging strain of influenza virus for diagnostic or therapeutic purposes comprising

(1) obtaining at least one isolate of each strain of a plurality of strains of influenza virus,

(2) analyzing the hemagglutinin amino acid sequence of the at least one isolate of each strain of the plurality of strains of influenza virus for the presence and concentration of Replikin sequences,

(3) comparing the concentration of Replikin sequences in the hemagglutinin amino acid sequence of the at least one isolate of each strain of the plurality of strains of influenza virus to the concentration of Replikin sequences observed in the hemagglutinin amino acid sequence of each of the strains at at least one earlier time period to provide the concentration of Replikins for at least two time periods, said at least one earlier time period being within about six months to about three years prior to step (1), and

(4) identifying the strain of influenza virus having the highest increase in concentration of Replikin sequences during the at least two time periods.

In yet another aspect of the invention, there is provided an influenza virus vaccine comprising at least one isolated Replikin present in the hemagglutinin protein of an emerging strain of influenza virus and a pharmaceutically acceptable carrier and/or adjuvant.

Also provided by the present invention is a method of preventing or treating influenza virus infection comprising administering to a patient in need thereof a vaccine comprising at least one isolated Replikin present in the hemagglutinin protein of an emerging strain of influenza virus and a pharmaceutically acceptable carrier and/or adjuvant.

In another aspect of the invention, there are provided vaccines and methods for preventing or treating malaria. The malaria vaccines comprise at least one isolated Plasmodium falciparum Replikin. The present invention also provides methods for treating or preventing malaria comprising administering to a patient an effective amount of a vaccine comprising at least one isolated Plasmodium falciparum Replikin.

Also provided by the present invention are antibodies, antibody cocktails and compositions that comprise antibodies that specifically bind to a Replikin or Replikins present in a malaria antigen of Plasmodium falciparum.

As used herein, the term “peptide” refers to a compound of two or more amino acids in which the carboxyl group of one is united with an amino group of another, forming a peptide bond. The term peptide is also used to denote the amino acid sequence encoding such a compound. Thus, a peptide sequence may be a subsequence of a larger polypeptide sequence. As used herein, a Replikin peptide is a peptide having 7 to about 50 amino acids comprising (1) at least one lysine residue located six to ten amino acid residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues. Similarly, a.replikin sequence is the amino acid sequence encoding such a peptide.

The phrase “emerging strain” as used herein refers to a strain of influenza virus identified as having an increasing concentration of Replikin sequences in its hemagglutinin and/or neuraminidase protein sequence, relative to the concentration of replikins in other strains of influenza virus. The increase in concentration occurs over a period of at least about six months, and preferably over a period of at least about one year, most preferably over a period of at least about three years or more.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a bar graph depicting the frequency of occurrence of replikins in various protein groups.

FIG. 2 is a graph depicting the percentage of malignin per milligram total membrane protein during anaerobic replication of glioblastoma cells.

FIG. 3 is a bar graph showing amount of antimalignin antibody produced in response to exposure to the recognin 16-mer.

FIG. 4A is a photograph of a blood smear taken with ordinary and fluorescent light. FIG. 4B is a photograph of a blood smear taken with ordinary and fluorescent light illustrating the presence of two leukemic cells. FIG. 4C is a photograph of a dense layer of glioma cells in the presence of antimalignin antibody. FIG. 4D and FIG. 4E are photographs of the layer of cells in FIG. 4C taken at 30 and 45 minutes following addition of antimalignin antibody.

FIG. 4F is a bar graph showing the inhibition of growth of small cell lung carcinoma cells in vitro by antimalignin antibody.

FIG. 5 is a plot of the amount of antimalignin antibody present in the serum of patients with benign or malignant breast disease pre-and post surgery.

FIG. 6 is a box diagram depicting an embodiment of the invention wherein a computer is used to carry out the 3-point-recognition method of identifying replikin sequences.

FIG. 7 is a-graph showing the concentration of Replikins observed in hemagglutinin of influenza B and influenza A strain, H1N1, on a year by year basis from 1918 through 2001.

FIG. 8 is a graph of the replikin concentration observed in hemagglutinin of influenza A strains, H2N2 and H3N2, as well as an emerging strain defined by its constituent Replikins, designated H3N2(R), on a year by year basis from 1950 to 2001.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides methods for predicting future epidemics or pandemics of influenza virus, and vaccines and methods of designing effective vaccines against influenza virus. Identification of a new family of small peptides related to the phenomenon of rapid replication, referred to herein as Replikins, provides new targets for influenza virus detection and influenza vaccine development. Identification of this new family of peptides also provides for the detection of malaria and provides new targets for malaria vaccine development.

The first Replikin sequence to be identified was the cancer cell Replikin found in a brain cancer protein, malignin, which was demonstrated to be enriched ten-fold during rapid anaerobic replication of glioblastoma multiforme (glioma) cells. (FIG. 2) Malignin is a 10 KDa portion of the 250 KDa glycoprotein 10B, which was isolated in vivo and in vitro from membranes of glioblastoma multiforme (glioma) cells. Hydrolysis and mass spectroscopy of malignin revealed a16-mer peptide sequence, ykagvaflhkkndide (SEQ ID NO.:4), which is referred to herein as the glioma Replikin and which includes the shorter peptide, kagvaflhkk (SEQ ID NO.: 1), both of which apparently are absent in the normal human genome.

Table 1 illustrates how the sequence of the glioma Replikin, the 16-mer peptide sequence, ykagvaflhlkndide (SEQ ID NO.: 4) was determined. TABLE 1 16-mer peptide sequence ykagvaflhkkndide obtained from malignin by hydrolysis and mass spectrometry Method By Which Fragment Obtained Auto- Auto- hydrolysis hydrolysis of malignin of immobilized Micro- Micro- Seq malignin on waved waved ID Fragment MH+ free in bromoacetyl 5 30 NO. Identified (mass) Sequence solution cellulose seconds seconds 19 1-3 381.21 ()yka(g) + 20 1-5 537.30 ()ykagv(a) + 21 2-6 445.28 (y)kagva(f) + 22 2-7 592.35 (Y)kagvaf(l) + 23  4-11 899.55 (a)gvaflhkk(n) + 24 5-7 336.19 (g)vaf(l) + 25 6-7 237.12 (v)af(l) + 26  6-10 615.36 (v)aflhk(k) + 27  6-10 615.36 (v)aflhk(k) + 28  6-12 857.50 (v)aflhkkn(d) + 29  6-12 857.50 (v)afhkkn(d) + 30 7-8 279.17 (a)fl(h) + 31 10-16 861.43 (h)kkndide() + 32 11-14 489.27 (k)kndi(d) + 33 12-15 476.2- (k)ndid(e) +

When the 16-mer glioma Replikin was synthesized and injected as a synthetic vaccine into rabbits, abundant antimalignin antibody was produced. (Bogoch et al., Cancer Detection and Prevention, 26(Supp. 1): 402 (2002). The concentration of antimalignin antibody in serum in vivo has been shown to relate quantitatively to the survival of cancer patients. (Bogoch et al., Protides of Biological Fluids, 31:739-747 (1984). In vitro antimalignin antibodies have been shown to be cytotoxic to cancer cells at a concentration of picograms (femtomolar) per cancer cell. (Bogoch et al., Cancer Detection and Prevention, 26(Supp. 1): 402 (2002).

Studies carried out by the inventors showed that the glioma Replikin is not represented in the normal healthy human genome. Consequently, a search for the origin and possible homologues of the Replikin sequence was undertaken by analysis of published sequences of various organisms.

By using the 16-mer glioma Replikin sequence as a template and constructing a recognition proteomic system to visually scan the amino acid sequences of proteins of several different organisms, a new class of peptides, the Replikins, was identified. The present invention provides a method for identifying nucleotide or amino acid sequences that include a Replikin sequence. The method is referred to herein as a 3-point-recognition method. By use of the “3-point recognition” method, described herein below, a new class of peptides was revealed in algae, yeast, fungi, amoebae, bacteria, plant and virus proteins having replication, transformation, or redox functions. Surprisingly, the Replikin peptides were found to be concentrated in larger ‘replicating’ and ‘transforming’ proteins (so designated by their investigators, See Table 2). No sequences were found to be identical to the malignin 16-mer peptide.

Table 2 illustrates several Replikin sequences that were identified by the 3-point recognition method of the invention. TABLE 2 Examples of Replikins in various organisms- prototype: Glioma Replikin* kagvaflhkk (SEQ ID No.:1) SEQ ID NO. Algae: 34 Caldophera prolifera kaskftkh 35 Isolepisprolifera kaqaetgeikgh Yeast: 36 Schizosaccharomyces ksfkypkkhk pombe 37 Oryza sativa kkaygnelhk 2 Sacch. cerevisiae hsikrelgiifdk replication binding protein Fungi: Isocitrate lyase kvdivthqk ICI l, Penicillium marneffei 38 DNA-dependent RNA kleedaayhrkk polymerase 11, Diseula dcstructiva 39 Ophiostoma novo- kvilpfrgnikgiffkh ulm 1, RNA in Dutch elm disease fungus 40 fungus Amoeba: 41 Entamoeba invadens, klilkgdlnkh histone H2B Bacteria: 42 Pribosomal protein ksvhaflk replication factor, Helicobacter pylori Replication- associated protein Staph. aureus 10 Mycoplasma kkektthnk pulmonic, chromosome replication 43 Macrophage kvhffqlkk infectivity potentiator, L. legionella 90 Bacillus anthracis kihlisvkk 91 Bacillus anthracis hvkkekeknk 92 Bacillus anthracis khivkievk 93 Bacillus anthracis kkkkikdiygkdallh 94 Bacillus anthracis kwekikqh 95 Bacillus anthracis kklqipppiepkkddiih 96 Bacillus anthracis hnryasnivesayllilnew- knnsqsdlikk 97 Bacillus anthracis havddyagylidknqadlv- tnskk 98 Bacillus anthracis haerlkvqknapk Plants: 44 Arabidopsis kdhdfdgdk thaliana, prolifera 45 Arabidopsis kmkglkqkkah thaliana, cytoplasmic ribosomal 46 Arabidopsis kelssttqeksh thaliana, DNA binding protein Viruses: 9 Replication kekkpskdeimrdiish associated protein A [Maize streak virus] 11 Bovine herpes virus hkinitngqk 4, DNA replication protein 12 Meleagrid hkdlyrllmk herpesvirus 1, replication binding protein 47 Feline hlkdyklvk immunodeficiency 3 Foot and Mouth hkqkivapvk Disease (O) 5 HIV Type 1 kcfncgkegh 7 HIV Type 2 kcwncgkegh 99 Small Pox Virus khynnitwyk (Variola) 100 Small Pox Virus kysqtgkeliih (Variola) 101 Small Pox Virus hyddvrikndivvsrck (Variola) 102 Small Pox Virus hrfldildski (Variola) 103 Small Pox Virus kerghnyyfek (Variola) Tumor 48 Rous sarcoma virus kklrhek Viruses: tyrosine-protein kinase 49 v-yes, avian kklrhdk sarcoma 50 c-yes, colon kklrhdk cancer, malignant melanoma 51 v-srcC, avian kklrhek sarcoma 52 c-src, colon, kklrhek mammary, panrereatic cancer 53 Neuroblastoma RAS kqahelak viral (v-ras) oncogene 54 VPI (major capsid kthrfskh protein) [Polyamavirus sp.] 55 Sindbis knlhekik 56 El [Human khrpllqlk papilloamavirus type 71] 57 v-erbB from AEV and kspnhvk c-erb 58 v-fms (feline knihlekk sarcoma) 59 c-fms (acute and knihlekk chronic myelomonoeytic tumors) 60 large t-antigen I kphlaqslek [Polyomavirus sp.] 61 middle t-antigen kqhrelkdk [Polyomavirus sp,]- 62 small t-antigen kqhrelkdk [Polyomavirus sp], 63 v-abl, murine acute kvpvlisptlkh leukemia 64 Human T-cell kslllevdkdish lymphotropic virus typo 2 65 c-kit, GI tumors, kagitimvkreyh small cell lung carcinoma 18 Hepatitis C hyppkpgcivpak Trans- 66 Transforming ksgkhlgk forming protein myb Proteins: 67 Transforming krreqlkhk protein myc, Burkitt lymphoma 68 Ras-related GTP- ksfevikvih binding protein 69 Transforming kkkhtvkk protein ras (teratocarcinoma) 70 TRAF-associated kaqkdhlsk NF · kB activator TANK 71 RFP transforming hlkrvkdlkk protein 72 Transforming kygspkhrlik protein D (S.C.) 73 Papilloma virus klkhilgkarfik type 11, transforming protein 74 Protein tryosine kgdhvkhykirk kinase (EC 2.7.1.112slk 75 Transforming keklrdvmvdrhk protein (axl(-)) 76 Transforming kldqarqqqllkkieh protein (N-myc) 77 Fibroblast growth kkgnrvsptmkvth factor 4 (Kaposi sarcoma) Cancer 78 Matrix keiplhfrk Cell metaloproteinase 7 Proteins: (uterine) 79 Transcription kkkphikk factor 7-like 80 Breast cancer ktrhdplak antigen NY-BR-87 81 BRCA-1-Associated khhpkdnlik Ring Domain Protein (breast) 82 ‘Autoantigen from khkrkkfrqk a breast tumor’ 83 Glioma Replikin kagvaflhkk (this study) 84 Ovarian cancer khkrkkfrqk antigen 85 EE L leukemia kkkskkhkdk 86 Proto-oncogene hksekpalprk tyrosine-protein kinase C-ABLE 87 Adenomatosis kkkkpsrlkgdnek polyposis coli 88 Gastric cancer ktkkgnrvsptmkvth transforming protein 89 Transforming khkekmskdgkkkkkksk protein (K-RAS 2B), lung

Identification of an amino acid sequence as a Replikin or as containing a Replikin, i.e., a homologue of the glioma peptide, kagvaflhkk, requires that the three following requirements be met. The peptide sequence must have (1) at least one lysine residue located six to ten residues from another lysine residue; (2) at least one histidine residue; and (3) a composition of at least 6% lysine within an amino acid sequence of 7 to about 50 residues.

Databases were searched using the National Library of Medicine keyword “PubMed” descriptor for protein sequences containing Replikin sequences. Over 4,000 protein sequences were visually examined for homologues. Sequences of all individual proteins within each group of PubMed-classified proteins were visually scanned for peptides meeting the three above-listed requirements. An infrequent occurrence of homologues was observed in “virus peptides” as a whole (1.5%) (N=953), and in other peptides not designated as associated with malignant transformation or replication such as “brain peptides” and “neuropeptides” (together 8.5%) (N=845). However, surprisin-gly, homologues were significantly more frequently identified in large “replicating proteins,” which were identified as having an established function in replication in bacteria, algae, and viruses. Even more surprising was the finding that Replikin homologues occurred in 100% of “tumor viruses” (N=250), in 97% of “cancer proteins” (N=401), and in 85% of “transforming viruses” (N=248). These results suggest that there are shared properties of cancer pathogenesis regardless of cell type and suggest a role of viruses in carcinogenesis, i.e., conversion of cells from a transformed albeit dormant state to a more virulent actively replicating state.

To permit classification of subtypes of Replikins, additional or “auxiliary specifications” to the basic “3-point-recognition” requirements may be added: (a) on a structural basis, such as the common occurrence of adjacent di- and polylysines in cancer cell proteins (e.g., transforming protein P21B(K-RAS 2B), lung, Table 2, SEQ ID NO.: 89), and other adjacent di-amino acids in TOLL-like receptors, or b) on a functional basis, such as exhibiting ATPase, tyrosine kinase or redox activity as seen in Table 2.

Whether Replikin structures are conserved or are subject to extensive natural mutation was examined by scanning the protein sequences of various isolates of foot and mouth disease virus (FMDV), where mutations in proteins of these viruses have been well documented worldwide for decades. Protein sequences of FMDV isolates were visually examined for the presence of both the entire Replikin and each of the component Replikin amino acid residues observed in a particular Replikin. For example, in the protein VP1 of FMDV type O, the Replikin (SEQ ID NO.: 3) “hkqkivapvk” was found to be conserved in 78% of the 236 isolates reported in PubMed, and each amino acid was found to be conserved in individual isolates as follows: his, 95.6%; lys, 91.8%; gln 92.3%; lys, 84.1%; ile, 90.7%; val, 91.8%; ala, 97.3%; pro, 96.2%; ala, 75.4%; and lys, 88.4%. The high rate of conservation suggests structural and fuictional stability of the Replikin structure. Similarly, sequence. conservation was observed in different isolates of HIV for its Replikins, such as (SEQ ID NO.: 5) “kcfncgkegh” or (SEQ ID NO.: 6) “kvylawvpahk” in HIV Type 1 and (SEQ ID NO.: 7) “kcwncgkegh” in HIV Type 2 (Table 2). Other examples of conservation are seen in the constant presence of malignin in successive generations, over ten years of tissue culture of glioma cells, and by the constancy of affinity of the glioma Replikin for antimalignin antibody isolated by immunoadsorption from 8,090 human sera from the U.S., U.K., Europe and Asia (e.g., FIG. 5 and U.S. Pat. No. 6,242,578 B 1).

As seen in FIG. 2, during anaerobic respiration when the rate of cell replication is increased, malignin is enriched. That is, malignin is found to increase not simply in proportion to the increase in cell number and total membrane proteins, but is enriched as much as tenfold in concentration, starting with 3% at rest and reaching 30% of total membrane protein. This clear demonstration of a marked increase in Replikin concentration with glioma cell replication points to and is consistent with the presence of Replikins here sought by the 3-point recognition method and found in the proteins of various organisms which were found by mutation studies and other previous studies to be critical to replication. For example, Replikins were identified in such proteins as “Saccharomyces cerevisiae replication binding protein” (SEQ ID NO.: 2) (hsikrelgiifdk); the “replication associated protein A of maize streak virus” (SEQ ID NO.: 8) (kyivcareahk) and (SEQ ID NO.: 9) (kekkpskdeimrdiish); the “replication-associated protein of Staphylococcus aureus” (SEQ ID NO.: 10) ( kkektthnk); the “DNA replication protein of bovine herpes virus 4” (SEQ ID NO.: 11) (hkinitngqk); and the “Mealigrid herpes virus 1 replication binding protein” (SEQ ID NO.: 12) (hkdlyrllmk). Previous studies of tomato leaf curl gemini virus show that the regulation of virus accumulation appears to involve binding of amino acids 1-160 of the “replicating protein” of that virus to leaf DNA and to other replication protein molecules during virus replication. Analysis of this sequence showed that amino acids 1-163 of this “replicating protein” contain five Replikins, namely: (SEQ ID NO.: 13) kfrinaknyfltyph, (SEQ ID NO.: 14) knletpvnklfiricrefh, (SEQ ID NO.: 15) hpniqaaksstdvk, (SEQ ID NO.: 16) ksstdvkaymdkdgdvldh, and (SEQ ID NO.: 17) kasalnilrekapkdfvlqfh.

Table 2 shows that Replikin-containing proteins also are associated frequently with redox functions, and protein synthesis or elongation, as well as with cell replication. The association with metal-based redox functions, the enrichment of the Replikin-containing glioma malignin concentration during anaerobic replication, and the cytotoxicity of antimaligrin at low concentrations (picograms/cell) (FIG. 4 c-f), all suggest that the Replikins are related to central respiratory functions, which are perhaps less often subjected to the mutations characteristic of proteins of more superficial location or less central survival function.

Of particular interest, it was-observed that at least one Replikin per 100 amino acids was found to be present in the hemagglutinin proteins of almost all of the individual strains of influenza viruses examined. The replikin sequences that were observed to occur in the hemagglutinin proteins of isolates of each of the four prevalent strains of influenza virus, influenza B, H1N1, H2N2, and H3N2, for each year that amino acid sequence data are available (1902-2001) are shown in Tables 3, 4, 5 and 6, below. TABLE 3 Replikin Sequences present in hemagglutinins of Influenza B viruses in each year for which amino acid sequences were available (1902-2001). Year Detected in Influenza B strain Influenza B Replikins (Peak in FIG. 7: EB1 EB2) kshfanlk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 104) kshfanlkgtk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 105) kshfanlkgtktrgklcpk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 106) hekyggink 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 107) hekygglnksk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 108) hekygglnkskpyytgehak 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 109) hakaigncpiwvk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 110) hakaigncpiwvktplklangtk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 111) hakaigncpiwvktplklangtkyrppak 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 112) hakaigncpiwvktplklangtkyrppakllk 1902,19,24,38,40,43,51,59,75,76,77,89,90,93,97,98,99,00,01 (SEQ ID NO. 113) hfanlkgtktrgk  1919,     76, 89,90,  99,00,01 (SEQ ID NO. 114) hfanlkgtktrgklcpk  1919,     76,   90,  99,00,01 (SEQ ID NO. 115) hsdneiqmvklygdsk 1919 (SEQ ID NO. 116) hsdneiqdknivklygdskpqk 1919 (SEQ ID NO. 117) hsdneiqmvklygdskpqk 1919, 24,         97,98, 00 (SEQ ID NO. 118) k(alv)silhevk 1919,  40,  59,    90,93 (SEQ ID NO. 119) kctgtipsakasilh 1919,         00 (SEQ ID NO. 120) kctgtipsakasilhevk 1919,       93 (SEQ ID NO. 121) kygglnkskpyytgeh 1919 (SEQ ID NO. 122) kvwcasgrskvikgslpligeadclh 1919, 38,40,43, 59,75,76,77,89,90,   98,99,00 (SEQ ID NO. 123) kpyytgehak 1919, 38,40,  59,    89,90,93,97,98,  01 (SEQ ID NO. 124) kcmgtipsakasilhevk 1924,   43,   75,76,77,   93 (SEQ ID NO. 125) hnvinaekapggpyk   1938,      93,97,  00 (SEQ ID NO. 126) hsdnetqmaklygdsk  1938,       93,97,  00 (SEQ ID NO. 127) hgvavaadlkstqeaink   1940,   59,        00 (SEQ ID NO. 128) hgvavaadlkstqeainkdtistqeaink 1940 (SEQ ID NO. 129) klygdskpqkftssangvtth   1943,   75,76,77,   93,97,   00 (SEQ ID NO. 130) hsdnetqmaklygdskpqk   1943,   75,76,77,   93 (SEQ ID NO. 131) hfanlkgtqtrgk      1959 (SEQ ID NO. 132) kprsalkckgfh         1988 (SEQ ID NO. 133) kskpyytgehakai(g/a)ncpiwvk            2000 (SEQ ID NO. 134) 1. Influenza B has not been responsible for any human pandemic (global distribution). 2. Abbreviation for years: eg. “19” = 1919, “01” = 2001. 3. The first year that a given replikin appears is indicated at the beginning of the series of years in which that replikin has been found. 4. Overlapping replikin sequences are listed separately. 5. Increase in number of new replikin structures occurs in years of epidemics (underlined): eg. 1951 and 1977 and correlates with increased total replikin concentration (number of replikins per 100 amino acid residues). See FIG. 7.

TABLE 4 H1N1 Replikin Sequences present in H1N1 hemagglutinins of Influenza viruses in each year for which amino acid sequences were available (1918-2000) Year Detected in Influenza H1N1 Replikin (Peak in FIG. 7: H1N1 Strain P1 E1 E1.1, 1.2, 1.3 E1.4) hp(v/i)tigecpkyv(r/k)(s/t)(t/a)k 1918,25,28,30,31,35,47,48,51,52,55,56, (SEQ ID NO. 135) 57,59,63,77,79,80,81,85,87,88,89,91,92, 95,96,97,98,99,00 hdsnvknly(e/g)kv(k/r)(n/s)ql(k/r)flflak   1918, 28,30,31,     (SEQ ID NO. 136)   77,79,80,   88, 91,  95,  98 hdsnvknly(e/g)kv(k/r)(n/s)qlk   1918, 28,30,31,     (SEQ ID NO. 137)   77,79,80,   88, 91,  95,  98 hkc(nn/dd)(a/t/e)cmesv(r/k)flgtydypkyseesklflre(e/k)idgvk   1918,  30, 35,   (SEQ ID NO. 138)     77, 80,           98 hkc(nn/dd)(a/t/e)cmesv(r/k)flgtydypkyseesk   1918,  30, 35,   (SEQ ID NO. 139)     77, 80,           98 hqn(e/g)qgsgyaadqkstqnai(d/n)gitflkvnsviekmntqftavgkefnklek 1918, 28,30,31,35,     (SEQ ID NO. 140)   59, 79,      95 hqn(e/g)qgsgyaadqkstqnai(d/n)gitnkvnsviek 1918, 28,30,31,35,     (SEQ ID NO. 141)   59, 79,       95 hqn(e/g)qgsgyaadqkstqnai(d/n)gitnk 1918, 28,30,31,35,     (SEQ ID NO. 142)   59, 79,       95 kfeifpktsswpnh 1918         (SEQ ID NO. 143)   77 kg(n/s/t)sypkl(n/s)ksy(v/t)nnkgkevlvlwgvh 1918    35,     (SEQ ID NO. 144)   77,      96 ksy(v/t)nnkgkevlvlwgvh 1918    35,     (SEQ ID NO. 145)   77,      96 hkcnnecmesvkngtydypkyseesklnrekidgvk   1928, 31,     (SEQ ID NO. 146)       95 hkcnnecmesvkngtydypkyseesk   1928, 31,     (SEQ ID NO. 147)       95 hkcnnecmesvkngtydypk   1928, 31,     (SEQ ID NO. 148)       95 hkcnnecmesvk   1928, 31,     (SEQ ID NO. 149)       95 hngkssfy(k/r)nllwlt(e/g)knglypnlsksyvnnkek   1928,       (SEQ ID NO. 150)     95,   00 hngkssfy(k/r)nllwlt(e/g)knglypnlsksyvnnk   1928, 31,     (SEQ ID NO. 151)       95,   00 hngkssfy(k/r)nllwlt(e/g)knglypnlsk   1928, 31,     (SEQ ID NO. 152)       95,   00 hngkssfy(k/r)nllwlt(e/g)k   1928, 31,     (SEQ ID NO. 153)       95,   00 kssfyknllwlteknglypnlsksyvnnkekevlvlwgvh   1928, 31,     (SEQ ID NO. 154)       95, knllwlteknglypnlsksyvnnkekevlvlwgvh   1928, 31,      (SEQ ID NO. 155)      95 knglypnlsksyvnnkekevlvlwgvh   1928, 31,     (SEQ ID NO. 156)       95,96,   00 ksy(v/a)nnkekev(l/-)(v/-)lwgvh   1928, 31,   51, (SEQ ID NO. 157)         95,96,  98, 00 kesswpnhtvtk   1928, 31,     (SEQ ID NO. 158)       95 het(t/n)kgvtaacpyagassfyrnllwlvkkensypklsksyvnnk   1930, 35 (SEQ ID NO. 159) het(t/n)kgvtaacpyagassfyrnllwlvkkensypklsk   1930, 35 (SEQ ID NO. 160) kfeifpktsswpnevlvlwgvh   1930 (SEQ ID NO. 161) kerswpkh    1947, 51,52,55,56,  (SEQ ID NO. 162)   79, 82 klsksyvnnkekevlvlwqvh    1947, 51 (SEQ ID NO. 163) knnkekevlvlwqvh    1947 (SEQ ID NO. 164) h(k/n)(g/q)kssfy(r/k)nllwltekng(l/s)yp(n/t)lsksyannkek     1948     (SEQ ID NO. 165)  79,    89,  96 h(k/n)(g/q)kssfy(r/k)nllwltek     1948     (SEQ ID NO. 166)  79,    89,  96 hakkssfyk     1951,  57,59 (SEQ ID NO. 167) hngklcrlkgk     1951,52,55,56,57,59, (SEQ ID NO. 168)  79, hyklnn(q/g)kk      1956,    (SEQ ID NO. 169)        00 hdiyrdeainnrfqiqgvkltqgyk        1956 (SEQ ID NO. 170) kgngcfeifhk        1956 (SEQ ID NO. 171) klnrliektndkyhqiek        1956 (SEQ ID NO. 172) klnrliektndkyh        1956 (SEQ ID NO. 173) kchtdkgslsttk        1956 (SEQ ID NO. 174) kinngdyaklyiwgvh        1956 (SEQ ID NO. 175) hngklcrkgiaplqlgk         1959, (SEQ ID NO. 176)   82 hetnrqvtaacpyagansffrnliwlvkkessypklsk         1963, (SEQ ID NO. 177)  81 hetnrqvtaacpyagansffrnliwlvkkessypklsk         1963, (SEQ ID NO. 178)  81 hpptstdqqslyqnadayifvgsskynrkfk         1963, (SEQ ID NO. 179)  81 hpptstdqqslyqnadayifvgsskynrkfkpeia         1963, (SEQ ID NO. 180)  81 hdiyrdeainnrfqiqgvkitqgyk           (SEQ ID NO. 181) 1977,79,    91 hqneqgsgyaadqkstqnaidgitnkvnsviekmntqftavgk           (SEQ ID NO. 182) 1977 hqneqgsgyaadqkstqnaidgitnkvnsviek           (SEQ ID NO. 183) 1977 hqneqgsgyaadqkstqnaingitnkvnsviekmntqftavgkefnklek           (SEQ ID NO. 184) 1979   91 hngklcrlkgiaplqlgk           (SEQ ID NO. 185) 1979 hkcnnecmesvk           (SEQ ID NO. 186) 1979 kfeifpkasswpnh           (SEQ ID NO. 187)  1981 hdsnvknlyekvrsqlrnnak           (SEQ ID NO. 188)  1981 kvnsvikkmntqfaavgkefnh           (SEQ ID NO. 189)  1981 klingklck           (SEQ ID NO. 190)  1981 kkgtsypklsksythnkgkevlvlwgvh           (SEQ ID NO. 191)  1981 kgtsypklsksythnkgkevlvlwgvh           (SEQ ID NO. 192)  1981 klsksythnkgkevlvlwgvh           (SEQ ID NO. 193)  1981 ksythnkgkevlvlwgvh           (SEQ ID NO. 194)  1981 kgvtascshk           (SEQ ID NO. 195)   1985,87 kgvtascshkgrssfyrnllwlteknglypnlsk           (SEQ ID NO. 196)   1985,87 kgnsypklsksyvnnkekevlvlwgih           (SEQ ID NO. 197)    1988 kefnhlek           (SEQ ID NO. 198)    1988 hpptstdqqslyqnadayvfvgsskynkkfkpeiatrpk           (SEQ ID NO. 199)    1988 hpptstdqqslyqnadayvfvgsskynkkfk           (SEQ ID NO. 200)    1988 hegkssfyrnllwltekegsypklknsyvnk           (SEQ ID NO. 201)     1991 hegkssfyrnllwltekegsypk           (SEQ ID NO. 202)     1991 hkcdnecmesvmgtydypkyseesk           (SEQ ID NO. 203)     1991 kesswpnhtvtk           (SEQ ID NO. 204)     1991,92 knllwlteknglypnlsksyvnnkekeilvlwgvh           (SEQ ID NO. 205)     1991,92, 96 hngkssfy(k/m)(n/-)llwlt(e/g)(-/k)knglypnlsk           (SEQ ID NO. 206)     1991,92, 96   00 hngkssfyknllwltek           (SEQ ID NO. 207)     1991,92, 96 htvtkgvtascshngkssfyknllwlteknglypnlsksyvnnkekevlvlwgvh           (SEQ ID NO. 208)      1995 htvt(k/g)gv(t/s)ascshngkssfy(k/m)(n/-)llwlt(e/g)k(-n/k)glypnlsk           (SEQ ID NO. 209)      1995,    00 htvtkgvtascshngkssfyknhlwltek           (SEQ ID NO. 210)      1995 kyvrstklrmvtglrnipsiqsrglfgaiagfieggwtgmidgwygyh           (SEQ ID NO. 211)      1995 hqneqgsgyaadqkstqnaingitnkvnsiiekmntqftavgk           (SEQ ID NO. 212)      1995 hqneqgsgyaadqkstqnaingitnkvnsiiek           (SEQ ID NO. 213)      1995 hqneqgsgyaadqkstqnaingitnk           (SEQ ID NO. 214)      1995 hsgarsfyrnllwivkkgnsypk           (SEQ ID NO. 215)       1996 hsgarsfyrnllwivkkgnsypklnk           (SEQ ID NO. 216)       1996 hsgarsfyrnllwivkkgnsypklnksytndk           (SEQ ID NO. 217)       1996 hsgarsfyrnllwivkkgnsypklnksytndkgk           (SEQ ID NO. 218)       1996 litvskgvttscshngk           (SEQ ID NO. 219)       1996 katswpnhettk           (SEQ ID NO. 220)       1996 kqvttscshnqk           (SEQ ID NO. 221)       1996 kgnsypklnksytndkgkevlviwgvh           (SEQ ID NO. 222)       1996 klnksytndkgkevlviwgvh           (SEQ ID NO. 223)       1996 ksytndkgkevlviwgvh           (SEQ ID NO. 224)       1996 hnqkssfyrnllwlt(e/q)knglypnlsksy(v/a)annkek           (SEQ ID NO. 225)        1997,98,99 hpitigecpkyvrsak           (SEQ ID NO. 226)        1997 hqneqgsgyaadqkstqnaingitnkvnsviekmntqftavgk           (SEQ ID NO. 227)         1998 hqneqgsgyaadqkstqnaingitnkvnsviek           (SEQ ID NO. 228)         1998 hngkssfyrnllwlteknglypnlsksyvnnkek           (SEQ ID NO. 229)         1998 1. Influenza H1N1 was responsible for the human pandemic (global distribution) of 1918. 2. Abbreviation for years: eg. “96” = 1996. 3. The first year that a given replikin appears is indicated at the beginning of the series of years in which that replikin has been found in this work. 4. Overlapping replikin sequences are listed separately. Increase in number of new replikin structures occurs in years of epidemics (underlined): eg. 1918 and 1977 and correlates with increased total replikin concentration (number of replikins per 100 amino acid residues). See FIG. 7.

TABLE 5 Replikin Sequences present in hemagglutinins of Influenza H2N2 viruses in years 1957-2000 Year Detected in Influenza H2N2 strain Influenza H2N2 Replikins (Peak in FIG. 8 P2 E2) khfekvkilpk 1957,58,59,60,61,64,65,68,   78,83,84,91 (SEQ ID NO. 230) khllssvkhfekvk 1957,58,59,60,61,      83,84,91 (SEQ ID NO. 231) ha(k/q/m)(d/n)ilekthngk 1957,58,59,60,61,64,65,68,   78,83,84, (SEQ ID NO. 232) 91, 95 ha(k/q/m)(d/n)ilekthngklc(k/r) 1957,58,59,60,61,64,65,68,   78,83,84, (SEQ ID NO. 233) 91, 95 hnvhpltigecpkyvksek 1957,58,59,   65,68 (SEQ ID NO. 234) hpltigecpkyvksek 1957,58,59,   65,68,64,65,68,78,83,84, (SEQ ID NO. 235) 91 khllssvkhfekvkilpk 1957,58,59,60,61,64,65,68,   78 (SEQ ID NO. 236) krqssgimktegtlencetkcqtplgainttlpfhnvh 1957, 59,      83 (SEQ ID NO. 237) kgsnyp(v/i)ak(g/r)synntsgeqmliiwq(v/i) 1957,58,59, 61,     83, 91, (SEQ ID NO. 238)  95 httlgqsracavsgnpsffrnmvwltekgsnypvak 1957 (SEQ ID NO. 239) klifekvk 1957, 59,  65 (SEQ ID NO. 240) kiskrgssgimkteglencetkcqtplgainttlpfh 1957, 59,  65,     91 (SEQ ID NO. 241) krgssgimkteglencetkcqtplgainttlpfh 1957, 59,  65,     91 (SEQ ID NO. 242) ktegtlencetkcqtplgainttlpfh 1957, 59,  65,     91 (SEQ ID NO. 243) kiskrgssgimkteglencetkcqtplgainttlpfh 1957, 59,  65,     91 (SEQ ID NO. 244) kteglencetkcqtplgainttlpfhn(v/i)h 1957, 59,  65,     91 (SEQ ID NO. 245) kiskrgssgimkteglencetkcqtplgainttlpfh 1957, 59,  65,     91 (SEQ ID NO. 246) k(e/g)snypvakgsynntsgeqmliiwgvh 1957,  60,  65 (SEQ ID NO. 247) hpitigecpkyvksek 1957,  60,  65 (SEQ ID NO. 248) kcqtplgaikttlpfh 1957,     65 (SEQ ID NO. 249) hhsndqgsgyaadkestqka(f/i)dgitnkvnsviek-    1961, 65,68,   83,84 mntqfeavgklf(n/s)nleklenlinkk (SEQ ID NO. 250) hsndqgsgyaadkestqka(f/i)dgitnkvnsiek-    1961, 65,68,   83,84 mntqfeavgklf(n/s)nleklenlnkk (SEQ ID NO. 251) hsndqgsgyaadkestqka(f/i)dgitnk    1961, 65,68,   83,84 (SEQ ID NO. 252) hdsnvrnlydkvrmqlrdnak     1964, 68,76,     (SEQ ID NO. 253) 84,91 hkcddecmnsvkngtydypklnmeikgvk     1964,65,68,76,   83,84, (SEQ ID NO. 254) 91 hkcddecmnsvkngtydypklnmeik     1964,65,68,76,   83,84, (SEQ ID NO. 255) 91 hkcddecmnsvkngtydypk     1964,65,68,76,   83,84, (SEQ ID NO. 256) 91 hkcddecmnsvk     1964,65,68,76,   83,84, (SEQ ID NO. 257) 91 kgsnypvakgsynntngeqiliiwgvh        1976,78 (SEQ ID NO. 258) hsndqgsgyaadkestqkavdgitnkvnsviekmntqfeavgk        1976,     (SEQ ID NO. 259) 91 krgssgimktegtlencetkcqtplgainttlpfh        1976,78,  83, (SEQ ID NO. 260) 84 hpltigecpkyvksek        1976 (SEQ ID NO. 261) hakdilekthngklck        1976 (SEQ ID NO. 262) 1. Influenza H2N2 was responsible for the human pandemic (global distribution) of 1957. 2. Abbreviation for years: eg. “58” = 1958. 3. The first year that a given replikin appears is indicated at the beginning of the series of years in which that replikin has been found.in this work. 4. Overlapping replikin sequences are listed separately. 5. Increase in number of new replikin structures occurs in years of epidemics (underlined): eg. 1957 and 1965 and correlates with increased total replikin concentration (number of replikins per 100 amino acid residues). See FIG. 8.

TABLE 6 H3N2 Replikin Sequences present in H3N2 hemagglutinins of Influenza viruses in each year for which amino acid sequences were available (1968-2000) Year Detected in Influenza H3N2 strain Influenza Replikins Influenza H3N2 Replikins (Peak in FIG. 8 P3 E3 E4) hdvyrdealnnrfqikgvelksgyk 1968,72, 75     96,97,98 (SEQ ID NO. 263) htidltdsemnklfertrk 1968 (SEQ ID NO. 264) kfhqiek 1968,72, 75, 77      96, (SEQ ID NO. 265) 97,98 ktnekfh(g/q)iek 1968      86   98 (SEQ ID NO. 266) klnr(v/l)iektnekfh 1968,72, 75, 77        (SEQ ID NO. 267) 97,98 hqiekefsevegriqdlekyvedtk 1968,72,         98 (SEQ ID NO. 268) kicnnphk   1975 (SEQ ID NO. 269) klnrvikktnekfh   1975 (SEQ ID NO. 270) hd(I,v)yrdealnnrfqik(g/q)ve(r/k)s(q/g)yk   1975,76,77,     86 (SEQ ID NO. 271) hqiekefsevegriqdlekyvedtk   1975 (SEQ ID NO. 272) kyvedtkidlwsynaellvalenqh   1975 (SEQ ID NO. 273) kyvkqnslklatgmrnvpekqtrglfgaiagfiengwegmidgwygfrh   1975 (SEQ ID NO. 274) kefsevegriqdlekyvedtkidlwsynaellvalenqh   1975      2000 (SEQ ID NO. 275) hqn(s/e)(e/q)g(t/s)g(q/y)aad(l/q)kstq(a/n)a(i/l)d-   1975      2000 (q/g)I(n/t)(g/n)k(l/v)n(r/s)vi(e/c)k (SEQ ID NO. 276) hcd(g/q)f(q,r)nekwdlf(v,/i)er(s/t)k 1975,76,77,78,80,81,82,83,84,85,86,88,89,90,91,92, (SEQ ID NO. 277) 93,94,95,96,97,98 htidltdsemnkklfertrk   1977, (SEQ ID NO. 278) ksgstypvlkvtmpnndflfdklyiwgvh   1977 (SEQ ID NO. 279) klnwltksgntypvlnvtmpnndnfdklviwgvh    1982 (SEQ ID NO. 280) htidltdsemnklfektrk     1986 (SEQ ID NO. 281) klnrliektnekfhqtek      1987 (SEQ ID NO. 282) htgkssvmrsdapidfcnsecitpnqsipndkpfqnvnkitygacpk       1994 (SEQ ID NO. 283) htgkssvmrsdapidfcnsecitpnqsipndkpfqnvnk       1994 (SEQ ID NO. 284) hpstdsdqtslyvrasgrvtvstkrsqqtvipk       1994 (SEQ ID NO. 285) kyvedtkidlwsynaellvalenqh        1997,98 (SEQ ID NO. 286) klfertrkqlrenaedmgngcfkiyh         1998 (SEQ ID NO. 287) krrsiksffsrlnwlh         1998 (SEQ ID NO. 288) hpvtigecpky(v/r)kstk          2000 (SEQ ID NO. 289) kgnsypklsklsksyiinkkkevlviwgih          2000 (SEQ ID NO. 290) klsklsks(v/y)iinkkkevlviwgih          2000 (SEQ ID NO. 291) klsks(v/y)iinkkkevlviwgih          2000 (SEQ ID NO. 292) 1. Influenza H3N2 was responsible for the human pandemic (global distribution) of 1968. 2. Abbreviation for years: eg. “77” = 1977. 3. The first year that a given replikin appears is indicated at the beginning of the series of years in which that replikin has been found. 4. Overlapping replikin sequences are listed separately. 5. Increase in number of new replikin structures occurs in years of epidemics (underlined): eg. 1975 and correlates with increased total replikin concentration (number of replikins per 100 amino acid residues). See FIG. 8.

Both the concentration and type, i.e., composition of Replikins observed were found to relate to the occurrence of influenza pandemics and epidemics. The concentration of Replikins in influenza viruses was examined by visually scanning the hemagglutinin amino acid sequences published in the National Library of Medicine “PubMed” data base for influenza strains isolated world wide from human and animal reservoirs year by year over the past century, i.e., 1900 to 2001. These Replikin concentrations (number of Replikins per 100 amino acids, mean ±SD) were then plotted for each strain.

The concentration of Replikins was found to directly relate to the occurrence of influenza pandemics and epidemics. The concentration of Replikins found in influenza B hemagglutinin and influenza A strain, H1N1, is shown in FIG. 7, and the concentration of Replikins found in the two other common influenza virus A strains, H2N2 and H3N2 is shown in FIG. 8 (H2N2, H3N2). The data in FIG. 8 also demonstrate an emerging new strain of influenza virus as defined by its constituent Replikins (H3N2(R)).

Each influenza A strain has been responsible for one pandemic: in 1918, 1957, and 1968, respectively. The data in FIGS. 7 and 8 show that at least one replikin per 100 amino acids is present in each of the influenza hemagglutinin proteins of all isolates of the four common influenza viruses examined, suggesting a function for Replikins in the maintenance of survival levels of replication. In the 1990s, during the decline of the H3N2 strain there were no Replikins present in many isolates of H3N2, but a high concentration of new replikins appeared in H3N2 isolates, which define the emergence of the H3N2(R) strain.

Several properties of Replikin concentration are seen in FIG. 7 and FIG. 8 to be common to all four influenza virus strains: (1) Concentration is cyclic over the years, with a single cycle of rise and fall occurring over a period of two to thirty years. This rise and fall is consistent with the known waxing and waning of individual influenza virus strain predominance by hemagglutinin and neuraminidase classification. (2) Peak Replikin concentrations of each influenza virus strain previously shown to be responsible for a pandemic were observed to relate specifically and individually to each of the three years of the pandemics. For example, for the pandemic of 1918, where the influenza virus strain, H1N1, was shown to be responsible, a peak concentration of the Replikins in H1N1 independently occurred (P1); for the pandemic of 1957, where H2N2 emerged and was shown to be responsible, a peak concentration of the Replikins in R2N2 occurred (P2); and for the pandemic of 1968, where H3N2 emerged and was shown to be the cause of the pandemic, a peak concentration of the Replikins in H3N2 occurred (P3). (3) In the years immediately following each of the above three pandemics, the specific Replikin concentration decreased markedly, perhaps reflecting the broadly distributed immunity generated in each case. Thus, this post-pandemic decline is specific for H1N1 immediately following the pandemic (P1) for which it was responsible, and is not a general property of all strains at the time. An increase of Replikin concentration in influenza B repeatedly occurred simultaneously with the decrease in Replikin concentration in H1N1, e.g., EB1 in 1951 and EB2 in 1976, both associated with influenza B epidemics having the highest mortality. (Stuart-Harris, et al., Edward Arnold Ltd. (1985). (4) A secondary peak concentration, which exceeded the primary peak increase in concentration, occurred 15 years after each of the three pandemics, and this secondary peak was accompanied by an epidemic: 15 years after the 1918 pandemic in an H1N1 ‘epidemic’ year (El); eight years after the 1957 pandemic in an H2N2 ‘epidemic’ year (E2); and occurred seven years after the 1968 pandemic in an H3N2 ‘epidemic’ year (E3). These secondary peak concentrations of specific Replikins may reflect recovery of the strain. (5) Peaks of each strain's specific Replikin concentration frequently appear to be associated with declines in Replikin concentration of one or both other strains, suggesting competition between strains for host sites. (6) There is an apparent overall tendency for the Replikin concentration of each strain to decline over a period of 35 years (H2N2) to 60 years (influenza B). This decline cannot be ascribed to the influence of vaccines because it was evident in the case of influenza B from 1901 to 1964, prior to common use of influenzavaccines. In the case of influenza B, Replikin recovery from the decline is seen to occur after 1965, but Replikin concentration declined again between 1997 and 2000 (FIG. 7), and this correlates with the low occurrence of influenza B in recent case isolates. H1N1 Replikin concentration peaked in 1978-1979 (FIG. 7) together with the reappearance and prevalence of the H1N1 strain, and then peaked in 1996 coincident with an H1N1 epidemic. (FIG. 7). H1N1 Replikin concentration also declined between 1997 and 2000, and the presence of H1N1 strains decreased in isolates obtained during these years. For H2N2 Replikins, recovery from a 35 year decline has not occurred (FIG. 8), and this correlates with the absence of H2N2 from recent isolates. For H3N2, the Replikin concentration of many isolates fell to zero during the period from 1996 to 2000, but other H3N2 isolates showed a significant, sharp increase in Replikin concentration. This indicates the emergence of a sub-strain of H3N2, which is designated herein as H3N2(R).

FIGS. 7 and 8 demonstrate that frequently a one to three year stepwise increase is observed before Replikin concentration reaches a peak. This stepwise increase proceeds the occurrence of an epidemic, which occurs concurrently with the Replikin peak. Thus, the stepwise increase in concentration of a particular strain is a signal that that particular strain is the most likely candidate to cause an epidemic or pandemic.

Currently, Replikin concentration in the H3N2(R) strain of influenza virus is increasing (FIG. 8, 1997 to 2000). Three similar previous peak increases in H3N2 Replikin concentration are seen to have occurred in the H3N2-based pandemic of 1968 (FIG. 8), when the strain first emerged, and in the H3N2-based epidemics of 1972 and 1975 (FIG. 8). Each of these pandemic and epidemics was associated with excess mortality. (Ailing, et al., Am J. Epidemiol., 113(1):30-43 (1981). The rapid ascent in concentration of the H3N2(R) subspecies of the H3N2 Replikins in 1997-2000, therefore, statistically represents an early warning of an approaching severe epidemic or pandemic. An H3N2 epidemic occurred in Russia in 2000 (FIG. 8, E4); and the CDC report of December 2001 states that currently, H3N2 is the most frequently isolated strain of influenza virus world wide. (Morbidity and Mortality Weekly Reports (MMWR), Center for Disease Control; 50(48):1084-68 (Dec. 7, 2001).

In each case of influenza virus pandemic or epidemic new Replikins emerge. There has been no observation of two of the same Replikins in a given hemagglutinin in a given isolate. To what degree the emergence of a new Replikin represents mutations versus transfer from another animal or avian pool is unknown. In some cases, each year one or more of the original Replikin structures is conserved, while at the same time, new Replikins emerge. For example, in influenza virus B hemagglutinin, five Replikins were constantly-conserved between 1919 and 2001, whereas 26 Replikins came and went during the same period (some recurred after several years absence). The disappearance and re-emergence years later of a particular Replikin structure suggests that the Replikins return from another virus host pool rather than through de novo mutation.

In the case of H1N1 Replikins, the two Replikins present in.the P1 peak associated with the 1918 pandemic were not present in the recovery E1 peak of 1933, which contains 12 new Replikins. Constantly conserved Replikins, therefore, are the best choice for vaccines, either alone or in combination. However, even recently appearing Replikins accompanying one year's increase in concentration frequently persist and increase further for an additional one or more years, culminating in a concentration peak and an epidemic, thus providing both an early warning and time to vaccinate with synthetic Replikins (see for example, H1N1 in the early 1990's, FIG. 7).

The data in FIGS. 7 and 8 demonstrate a direct relationship between the presence and concentration of a particular Replikin in influenza protein sequences and the occurrence of pandemics and epidemics of influenza. Thus, analysis of the influenza virus hemagglutinin protein sequence for the presence and concentration of Replikins provides a predictor of influenza pandemics and/or epidemics, as well as a target for influenza vaccine formulation.

Composition of Replikins in Strains of Influenza Virus B: Of a total of 26 Replikins identified in this strain (Table 3), the following ten Replikins are present in every influenza B isolate examined from 1902-2001. Overlapping Replikin sequences are listed separately. Lysines and histidines are in bold type to demonstrate homology consistent with the “3-point recognition.” kshfanlk (SEQ ID NO. 104) kshfanlkgtk (SEQ ID NO. 105) kshfanlkgtktrgklcpk (SEQ ID NO. 106) hekyggink (SEQ ID NO. 107) hekygglnksk (SEQ ID NO. 108) hekygglnkskpyytgehak (SEQ ID NO. 10) hakaigncpiwvk (SEQ ID NO. 110) hakaigncpiwvvkktplklangtk (SEQ ID NO. 111) hakaigncpiwvktplklangtkyrppak (SEQ ID NO. 112) hakaigncpiwvktplklangtkyrppakllk (SEQ ID NO. 113)

Tables 3 and 4 indicate that there appears to be much greater stability of the Replikin structures in influenza B hemagglutinins compared with H1N1 Replikins. Influenza B has not been responsible for any pandemic, and it appears not to have an animal or avian reservoirs. (Stuart-Harris et al., Edward Arnold Ltd., London (1985)).

Influenza H1N1 Replikins: Only one replikin “hp(v/i)tigecpkyv(r/k)(s/t)(t/a)k” is present in every H1N1 isolate for which sequences are available from 1918, when the strain first appeared and caused the pandemic of that year, through 2000. (Table 4). (“(v/i)” indicates that the amino acid v or i is present in the same position in different years.) Although H1N1 contains only one persistent replikin, H1N1 appears to be more prolific than influenza B. There are 95 different replikin structures in 82 years on H1N1 versus only 31 different Replikins in 100 years of influenza B isolates (Table 4). An increase in the number of new Replikin structures occurs in years of epidemics. (Tables 3, 4, 5 and 6) and correlates with increased total Replikin concentration (FIGS. 7 and 8).

Influenza H2N2 Replikins: Influenza H2N2 was-responsible for the human pandemic of 1957. Three of the 20 Replikins identified in that strain for 1957 were conserved in each of the H2N2 isolates available for examination on PubMed until 1995 (Table 5). (SEQ ID NO. 232) ha(k/q/m)(d/n)ilekthngk (SEQ ID NO. 233) ha(k/q/m)(d/n)ilekthngklc(k/r) (SEQ ID NO. 238) kgsnyp(v/i)ak(g/r)synntsgeqmliiwq(v/i)h

However, in contrast to H1N1, only 13 additional Replikins have been found in H2N2 beginning in 1961. This paucity of appearance of new Replikins correlates with the decline in the concentration of the H2N2 Replikins and the appearance of H2N2 in isolates over the years. (FIG. 8).

Influenza H3N2 Replikins: Influenza H3N2 was responsible for the human pandemic of 1968. Five Replikins which appeared in 1968 disappeared after 1977, but reappeared in the 1990s (Table 6). The only Replikin structure which persisted for 22 years was hcd(g/q)f(q/r)nekwdlf(v/i)er(s/t)k, which appeared first in 1977 and persisted through 1998. The emergence of twelve new H3N2 replikins in the mid 1990s (Table 6) correlates with the increase in Replikin concentration at the same time (FIG. 8), and with the prevalence of the H3N2 strain in recent isolates together with the concurrent disappearance of all Replikins from some of these isolates (FIG. 8), this suggests the emergence of the new substrain H3N2(R).

FIGS. 1 and 2 show that influenza epidemics and pandemics correlate with the increased concentration of replikins in influenza virus, which is due to the reappearance of at least one replikin from one to 59 years after its disappearance. Also, in the A strain-only, there is an emergence of new strain-specific Replikin compositions (Tables 4-6). Increase in Replikin concentration by repetition of individual replikins within a single protein appears not to occur in influenza virus, but is seen in other organisms.

It has been believed that changes in the activity of different influenza strains are related to sequence changes in influenza hemagglutinins, which in turn are the products of substitutions effected by one of two poorly understood processes: i) antigenic drift, thought to be due to the accumulation of a series of point mutations in the hemagglutinin molecule, or ii) antigenic shift, in which the changes are so great that genetic reassortment is postulated to occur between the viruses of human and non-human hosts. First, the present data suggests that the change in activity of different influenza strains, rather than being related to non-specific sequence changes, are based upon, or relate to the increased concentration of strain-specific replikins and strain-specific increases in the replication associated with epidemics. In addition, the data were examined for a possible insight into which sequence changes are due to “drift” or “shift”, and which due to conservation, storage in reservoirs, then reappearance. The data show that the epidemic-related increase in replikin concentration is not due to the duplication of existing replikins per hemagglutinin, but is due to the reappearance of at least one replikin composition from 1 to up to 59 years after its disappearance, plus in the A strains only, the emergence of new strain-specific replikin compositions (Tables 3-6). Thus the increase in replikin concentration in the influenza B epidemics of 1951 and 1977 are not associated with the emergence of new replikin compositions in the year of the epidemic but only with the reappearance of replikin compositions which had appeared in previous years then disappeared (Table 3). In contrast, for the A strains, in addition to the reappearance of previously disappeared virus replikins, new compositions appear (e.g. in H1N1 in the year of the epidemic of 1996, in addition to the reappearance of 6 earlier replikins, 10 new compositions emerged). Since the A strains only, not influenza B, have access to non-human animal and avian reservoirs, totally new compositions probably derive from non-human host reservoirs rather than from mutations of existing human replikins which appear to bear no resemblance to the new compositions other than the basic requirements of “3-point recognition” (Tables 2-5). The more prolific nature of H1N1 compared with B, and the fact that pandemics have been produced by the three A strains only, but not by the B strain, both may also be a function of the ability of the human A strains to receive new replikin compositions from non-human viral reservoirs.

Some replikins have appeared in only one year, disappeared, and not reappeared to date (Tables 3-6). Other replikins disappear for from one to up to 81 years, when the identical replikin sequence reappears. Key replikin ‘k’ and ‘h’ amino acids, and the spaces between them, are conserved during the constant presence of particular replikins over many years, as shown in Tables 23-6for the following strain-specific replikins: ten of influenza B, the single replikin of H1N1, and the single replikin of H2N3, as well as for the reappearance of identical replikins after an absence. Despite the marked replacement or substitution activity of other amino acids both inside the replikin structure and outside it in the rest of the hemagglutinin sequences, influenza replikin histidine (h) appears never to be, and lysine (k) is rarely replaced. Examples of this conservation are seen in the H1N1 replikin “hp(v/i)tigecpkyv(r/k)(s/t)(t/a)k,” (SEQ ID NO. 135) constant between 1918 and 2000, in the H3N2 replikin “hcd(g/q)f(q,r)nekwdlf(v/i)er(s/t)k” (SEQ ID NO. 277) constant between 1975 and 1998 and in the H3N2 replikin “bqn(s/e)(e/q)g(t/s)g(q/y)aad(l/q)kstq(a/n)a(i/l)d(q/g)I(n/t)(g/n)k,(l/v)n(r/s)vi(e/c)k” (SEQ ID NO. 276) which first appeared in 1975, disappeared for 25 years, and then reappeared in 2000. While many amino acids were substituted, the basic replikin structure of 2 Iysines, 6 to 10 residues apart, one histidine, a minimum of 6% lysine in not more than approximately 50 amino acids, was conserved.

Totally random substitution would not permit the persistence of these H1N1 and H3N2 replikins, nor from 1902 to 2001 in influenza B the persistence of 10 replikin structures, nor the reappearance in 1993 of a 1919 18mer replikin after an absence of 74 years. Rather than a random type of substitution, the constancy suggests an orderly controlled process, or in the least, protection of the key replikin residues so that they are fixed or bound in some way: lysines, perhaps bound to nucleic acids, and histidines, perhaps bound to respiratory redox enzymes. The mechanisms which control this conservation are at present unknown.

Whether the conservation of replikin structures is unique to influenza or occurs in other virus replikins was examined in foot and mouth disease virus (FMDV) isolates, where extensive mutations in proteins of this virus have been well-documented worldwide over decades. In the protein VP1 of FMDV type 0, the replikin “hkqkivapvk” (SEQ ID NO. 3) was found to be conserved in 78% of the 236 isolates reported in PubMed, and each amino acid was found to be conserved in individual isolates as follows: h,95.6%; k,91.8%; q,92.3%; k,84.1%; i,90.7%; v,91.8%; a.97.3%; p,96.2%; a,75.4%; k,88.4%. Similarly, conservation was observed in different isolates of HIV for its replikins such as “kcfncgkegh” (SEQ ID NO. 5) or “kvylawvpahk” (SEQ ID NO. 6) in HIV Type 1 and “kcwncgkegh” (SEQ ID NO. 7) in HIV Type 216. The high rate of conservation observed in FMVD and HIV replikins suggests that conservation observed in influenza replikins is a general property of viral replikins.

Data on anti-Replikin antibodies also support Replikin class unity. An anti-Replikin antibody response has been quantified by immunoadsorption of serum antimalignin antibody to immobilized malignin (see Methods in U.S. Pat. No. 5,866,690). The abundant production of antimalignin antibody by administration to rabbits of the synthetic version of the 16-mer peptide whose sequence was derived from malignin, absent carbohydrate or other groups, has established rigorously that this peptide alone is an epitope, that is, it is a sufficient basis for this immune response (FIG. 3). The 16-mer peptide produced both IgM and IgG forms of the antibody. Antimalignin antibody was found to be increased in concentration in serum in 37% of 79 cases in the U.S. and Asia of hepatitis B and C, early, in the first five years of infection, long before the usual observance of liver cancer, which develops about fifteen to twenty-five years after infection. Relevant to both infectious hepatitis and HIV infections, transformed cells may be one form of safe haven for the virus: prolonging cell life and avoiding virus eviction, so that the virus remains inaccessible to anti-viral treatment.

Because administration of Replikins stimulates the immune system to produce antibodies having a cytotoxic effect, peptide vaccines based on the particular influenza virus Replikin or group of Replikins observed to be most concentrated over a given time period provide protection against the particular strain of influenza most likely to cause an outbreak in a given influenza season., e.g., an emerging strain or re-emerging strain For example, analysis of the influenza virus hemagglutinin amino acid sequence on a yearly or bi-yearly basis, provides data which are useful in formulating a specifically targeted influenza vaccine for that year. It is understood that such analysis may be conducted on a region-by-region basis or at any desired time period, so that strains emerging in different areas throughout-the world can be detected and specifically targeted vaccines for each region can be formulated.

Currently, vaccine formulations are changed twice yearly at international WHO and CDC meetings. Vaccine formulations are based on serological evidence of the most current preponderance of influenza virus strain in a given region of the world. However, prior to the present invention there has been no correlation of influenza virus strain specific amino acid sequence changes with occurrence of influenza epidemics or pandemics.

The observations of specific Replikins and their concentration in influenza virus proteins provides the first specific quantitative early chemical correlates of influenza pandemics and epidemics and provides for production and timely administration of influenza vaccines tailored specifically to treat the prevalent emerging or re-emerging strain of influenza virus in a particular region of the world. By analyzing the protein sequences of isolates of strains of influenza virus, such as the hemagglutinin protein sequence, for the presence, concentration and/or conservation of Replikins, influenza virus pandemics and epidemics can be predicted. Furthermore, the severity of such outbreaks of influenza can be significantly lessened by administering an influenza peptide vaccine based on the Replikin sequences found to be most abundant or shown to be on the rise in virus isolates over a given time period, such as about one to about three years.

An influenza peptide vaccine of the invention may include a single Replikin peptide sequence or may include a plurality of Replikin sequences observed in influenza virus strains. Preferably, the peptide vaccine is based on Replikin sequence(s) shown to be increasing in concentration over a given time period and conserved for at least that period of time. However, a vaccine may include a conserved Replikin peptide(s) in combination with a new Replikin(s) peptide or may be based on new Replikin peptide sequences. The Replikin peptides can be synthesized by any method, including chemical synthesis or recombinant gene technology, and may include non-Replikin sequences, although vaccines based on peptides containing only Replikin sequences are preferred. Preferably, vaccine compositions of the invention also contain a pharmaceutically acceptable carrier and/or adjuvant.

The influenza vaccines of the present invention can be administered alone or in combination with antiviral drugs, such as ganciclovir; interferon; interleukin; M2 inhibitors, such as, amantadine, rimantadine; neuraminidase inhibitors, such as zanamivir and oseltamivir; and the like, as well as with combinations of antiviral drugs.

Analysis of the primary structure of a Plasmodium farciparum malaria antigen located at the merozoite surface and/or within the parasitophorous vacuole revealed that this organism, like influenza virus, also contains numerous Replikins. However, there are several differences between the observation of Replikins in Plasmodium falciparum and influenza virus isolates. For example, Plasmodium falciparum contains several partial Replikins, referred to herein as “Replikin decoys.” These decoy structures contain an abundance of lysine residues, but lack the histidine required of Replikin structures. It is believed that the decoy structure maximizes the chances that an anti-malarial antibody or other agent will bind to the relatively less important structure containing the lysines, i.e., the Replikin decoys, rather than binding to histidine, which is present in Replikin structure, such as replilins in respiratory enzymes, which could result in destruction of the trypanosome.

Another difference seen in Plasmodium falciparum is a frequent repetition of individual Replikin structures within a single protein, which was not observed with influenza virus. Repitition may occur by (a) sharing of lysine residues between Replikins, and (b) by repetition of a portion of a Replikin sequence within another Replikin sequence.

A third significant difference between Replikin structures observed in influenza virus isolates and Plasmodium falciparum is a marked overlapping of Replikin structures throughout malarial proteins, e.g., there are nine overlapping replikins in the 39 amino acid sequence of SEQ ID NO. 393 (Replikin concentration=23.1/100 amino acids); and 15 overlapping replikins in the 41 amino acids of SEQ ID NO. 467 (Replikin concentration 36.6/100 amino acids). Both of these overlapping Replikin structures occur in blood stage trophozoites and schizonts. In contrast, influenza virus Replikins are more scattered throughout the protein and the maximum Replikin concentration is about 7.5/100 amino acids (FIG. 7); and tomato leaf curl gemini virus, which was also observed to have overlapping replikins has only about 3.1/100 amino acids.

This mechanism of lysine multiples is also seen in the Replikins of cancer proteins such as in gastric cancer transforming protein, ktkkgnrvsptmkvth (SEQ ID NO. 88), and in transforming protein P21B (K-RAS 2B) of lung, khkekmskdgkkkkkks (SEQ ID NO. 89).

The relationship of higher Replikin concentration to rapid replication is also confirmed by-analysis of HIV isolates. It was found that the slow-growing low titer strain of HIV (NSI, “Bru”, which is prevalent in early stage HIV infection has a Replikin concentration of 1.1 (±1.6) Replikins per 100 amino acids, whereas the rapidly-growing high titer strain of HrV (S1, “Lai”), which is prevalent in late stage HIV infection has a Replikin concentration of 6.8 (±2.7) Replikins per 100 amino acid residues.

The high concentration of overlapping Replikins in malaria, influenza virus and cancer cells is consistent with the legendary high and rapid replicating ability of malaria organisms. The multitude of overlapping Replikins in malaria also provides an opportunity for the organism to flood and confuse the immune system of its host and thereby maximize the chance that the wrong antibody will be made and perpetuated, leaving key malaria antigens unharmed.

As in the case of influenza virus, for example, peptide vaccines based on the Replikin structure(s) found in the malaria organism can provide an effective means of preventing and/or treating malaria. Vaccination against malaria can be achieved by administering a composition containing one or a mixture of Replikin structures observed in Plasmodium falciparum. Furthermore, antibodies to malaria Replikins can be generated and administered for passive immunity or malaria detection purposes.

Table 7 provides a list of several Plasmodium falciparum Replikin sequences. It should be noted that this list is not meant to be complete. Different isolates of the organism may contain other Replikin structures. TABLE 7 Malaria replikins a) Primary structure of a Plasmodium falciparum malaria antigen located at the merozoite surface and within the parasitophorous vacuole a) i) DECOYS: (C-Terminal) keeeekekekekekeekekeekekeekekekeek (SEQ ID NO. 293) ekekeekeeekk, or keeeekekekekekeekekeekekeekekekeek (SEQ ID NO. 294) ekekeekeeekkek, or keeeekekekekekeekekeekekekeekekeek (SEQ ID NO. 295) ekeekeekeeekk, or keeeekekek (SEQ ID NO. 296) ii) REPLIKINS: Hkklikalkkniesiqnkk (SEQ ID NO. 297) hkklikalkkniesiqnkm (SEQ ID NO. 298) hkklikalkk (SEQ ID NO. 299) hkklikalk (SEQ ID NO. 300) katysfvntkkkiislksqghkk (SEQ ID NO. 301) katysfvntkkkiislksqghk (SEQ ID NO. 302) katysfvntkkkiislksqgh (SEQ ID NO. 303) htyvkgkkapsdpqca dikeeckellkek (SEQ ID NO. 304) kiislksqghk (SEQ ID NO. 305) kkkkfeplkngnvsetiklih (SEQ ID NO. 306) kkkfeplkngnvsetiklih (SEQ ID NO. 307) kkfeplkngnvsetiklih (SEQ ID NO. 308) kngnvsetildih (SEQ ID NO. 309) klihlgnkdkk (SEQ ID NO. 310) kvkkigvtlkkfeplldngnvsetiklihlgflk (SEQ ID NO. 311) dkkh hliyknksynplllscvkkmnmlkenvdyiqnqn (SEQ ID NO. 312) lfkelmnqkatysfvntkkkiislk hliyknksynplllscvkkmnmlkenvdyiqnqn (SEQ ID NO. 313) lfkelmnqkatysfvntk hliyknksynplllscvkkmnmlkenvdyiqnqn (SEQ ID NO. 314) lfkehmnqk hliyknksynplllscvkkmnmlkenvdyiqknq (SEQ ID NO. 315) nlfk hliyknksynplllscvkkmnmlk (SEQ ID NO. 316) ksannsanngkknnaeemknlvnflqshkklika (SEQ ID NO. 317) lkkniesiqnkkh kknnaeemknlvnflqshkklikalkkniesiqn (SEQ ID NO. 318) kkh knlvnflqshkklikalkkniesiqnkkh (SEQ ID NO. 319) kklikalkkniesiqnkkh (SEQ ID NO. 320) klikalkkniesiqnkkh (SEQ ID NO. 321) kkniesiqnkkh (SEQ ID NO. 322) kniesiqnkkh (SEQ ID NO. 323) knnaeemknlvnflqsh (SEQ ID NO. 324) kklikalkkniesiqnkkqghkk (SEQ ID NO. 325) kknnaeemknlvnflqshk (SEQ ID NO. 326) knnaeemknlvnflqsh (SEQ ID NO. 327) klikalkkniesiqnkkqghkk (SEQ ID NO. 328) kvkkigvtlkkfeplkngnvsetiklih (SEQ ID NO. 329) kngnvsetiklih (SEQ ID NO. 330) klihlgnkdkk (SEQ ID NO. 331) ksannsanngkknnaeemknlvnflqsh (SEQ ID NO. 332) kknnaeemknlvnflqsh (SEQ ID NO. 333) kklikalkkniesiqnkkh (SEQ ID NO. 334) kalkkniesiqnkkh (SEQ ID NO. 335) kkniesiqnkkh (SEQ ID NO. 336) kelmnqkatysfvntkkkiislksqgh (SEQ ID NO. 337) ksqghkk (SEQ ID NO. 338) kkkiislksqgh (SEQ ID NO. 339) kkiislksqgh (SEQ ID NO. 340) kkniesiqnkkh (SEQ ID NO. 341) kniesiqnkkh (SEQ ID NO. 342) htyvkgkkapsdpqcadikeeckellkek (SEQ ID NO. 343) htyvkgkkapsdpqcadlkeeckellk (SEQ ID NO. 344) b) “liver stage antigen-3” gene = “LSA-3” Replikins henvlsaalentqseeekkevidvieevk (SEQ ID NO. 345) kenvvttilekveettaesvttfsnileeiqent (SEQ ID NO. 346) itndtieekleelh hylqqmkekfskek (SEQ ID NO. 347) hylqqmkekfskeknnnvievtnkaekkgnvqvt (SEQ ID NO. 348) nktekttk hylqqmkekfskeknnnvievtnkaekkgnvqvt (SEQ ID NO. 349) nktekttkvdknnk hylqqmkekfskeknnnvievtnkaekkgnvqvt (SEQ ID NO. 350) nktekttkvdknnkvpkkrrtqk hylqqmkekfskeknnnvievtnkaekkgnvqvt (SEQ ID NO. 351) nktekttkvdknnkvpkkrrtqksk hvdevmkyvqkidkevdkevskaleskndvtnvl (SEQ ID NO. 352) kqnqdffskvknfvkkyk hvdevmkyvqkidkevdkevskaleskndvtnvl (SEQ ID NO. 353) kqnqdffskvknfvkk hvdevmkyvqkidkevdkevskaleskndvtnvl (SEQ ID NO. 354) kqnqdffsk hvdevmkyvqkidkevdkevskaleskndvtnvl (SEQ ID NO. 355) k hvdevmkyvqkidkevdkevskalesk (SEQ ID NO. 356) hvdevmkyvqkidkevdkevsk (SEQ ID NO. 357) hvdevmkyvqkidkevdk (SEQ ID NO. 358) hvdevmkyvqkidk (SEQ ID NO. 359) kdevidlivqkekriekvkakkkklekkveegvs (SEQ ID NO. 360) glkkh kvkakkkklekkveegvsglkkh (SEQ ID NO. 361) kakkkklekkveegvsglkkh (SEQ ID NO. 362) kkkklekkveegvsglkkh (SEQ ID NO. 363) kkklekkveegvsglkkh (SEQ ID NO. 364) kklekkveegvsglkkh (SEQ ID NO. 365) klekkveegvsglkkh (SEQ ID NO. 366) kkveegvsglkkh (SEQ ID NO. 367) kveegvsglkkh (SEQ ID NO. 368) hveqnvyvdvdvpamkdqflgilneagglkemff (SEQ ID NO. 369) nledvfksesdvitveeikdepvqk hikgleeddleevddlkgsildmlkgdmelgdmd (SEQ ID NO. 370) kesledvttklgerveslk hikgleeddleevddlkgsildmlkgdmelgdmd (SEQ ID NO. 371) kesledvttk hikgleeddleevddlkgsildmlkgdmelgdmd (SEQ ID NO. 372) k hikgleeddleevddlkgsildmlk (SEQ ID NO. 373) hiisgdadvlssalgmdeeqmktrkkaqrpk (SEQ ID NO. 374) hditttldevvellcdveedkiek (SEQ 1D NO. 375) kkleevhelk (SEQ ID NO. 376) kleevhelk (SEQ ID NO. 377) ktietdileekkkeiekdh (SEQ ID NO. 378) kkeiekdhfek (SEQ ID NO. 379) kdhfek (SEQ ID NO. 380) kfeeeaeeikh (SEQ ID NO. 381) c) 28 KDA ookinete surface antigen precursor Replikins: kdgdtkctlecaqgkkcikhksdhnhksdhnhks (SEQ ID NO. 382) dpnhkkknnnnnk kdgdtkctlecaqgkkcikhksdhnhksdhnhks (SEQ ID NO. 383) dpnhkk kdgdtkctlecaqgkkcikhksdhnhksdhnhks (SEQ ID NO. 384) dpnhk kdgdtkctlecaqgkkcikhksdhnhksdhnhk (SEQ ID NO. 385) kdgdtkctlecaqgkkcikhksdhnhk (SEQ ID NO. 386) kdgdtkctlecaqgkkcikhk (SEQ ID NO. 387) kdgdtkctlecaqgkk (SEQ ID NO. 388) kdgdtkctlecaqgk (SEQ ID NO. 389) kciqaecnykecgeqkcvwdgih (SEQ ID NO. 390) kecgeqkcvwdgih (SEQ ID NO. 391) hieckcnndyvltnryecepknkctsledtnk (SEQ ID NO. 392) d) Blood stage trophozoites and schizonts Replikins: ksdhnhksdhnhksdhnhksdhnhksdpnhkkkn (SEQ ID NO. 393) nnnnk ksdhnhksdhnhksdhnhksdpnhkkknnnnnk (SEQ ID NO. 394) ksdhnhksdhnhksdpnhkkknnnnnk (SEQ ID NO. 395) ksdhnhksdpnhkkknnnnnk (SEQ ID NO. 396) kkknnnnnkdnksdpnhk (SEQ ID NO. 397) kknnnnnkdnksdpnhk (SEQ ID NO. 398) knnnnnkdnksdpnhk (SEQ ID NO. 399) kdnksdpnhk (SEQ ID NO. 400) ksdpnhk (SEQ ID NO. 401) hslyalqqneeyqkvknekdqneikkikqliekn (SEQ ID NO. 402) k hslyalqqneeyqkvknekdqneikkik (SEQ ID NO. 403) hslyalqqneeyqkvknekdqneikk (SEQ ID NO. 404) hslyalqqneeyqkvknekdqneik (SEQ ID NO. 405) hklenleemdk (SEQ ID NO. 406) khfddntneqk (SEQ ID NO. 407) kkeddekh (SEQ ID NO. 408) keennkkeddekh (SEQ ID NO. 409) ktssgihikeennkkeddekh (SEQ ID NO. 410) knihikk (SEQ ID NO. 411) hikkkegidigyk (SEQ ID NO. 412) kkmwtcklwdnkgneitknih (SEQ ID NO. 413) kkgiqwnllkkmwtcklwdnkgneitknih (SEQ ID NO. 414) kekkdsnenrkkkqkedkknpnklkkieytnkit (SEQ ID NO. 415) hffkaknnkqqnnvth kkdsnenrkkkqkedkknpnklkkieytnkithf (SEQ ID NO. 416) fkaknnkqqnnvth kdsnenrkkkqkedkknpnklkkieytnkithff (SEQ ID NO. 417) kaknnkqqnnvth kkqkedkknpnklkkieytnkithffkaknnkqq (SEQ ID NO. 418) nnvth kqkedkknpnklkkieytnkithffkaknnkqqn (SEQ ID NO. 419) nvth kedkknpnklkkieytnkithffkaknnkqqnnv (SEQ ID NO. 420) th knpnklkkieytnkithffkaknnkqqnnvth (SEQ ID NO. 421) kkieytnkithffkaknnkqqnnvth (SEQ ID NO. 422) kieytnkithffkaknnkqqnnvth (SEQ ID NO. 423) kithffkaknnkqqnnvth (SEQ ID NO. 424) hknnedikndnskdikndnskdikndnskdiknd (SEQ ID NO. 425) nnedikndnskdik hknnedikndnskdikndnskdikndnskdiknd (SEQ ID NO. 426) nnedikndnsk hknnedikndnskdikndnskdikndnskdiknd (SEQ ID NO. 427) nnedik hknnedikndnskdikndnskdikndnskdik (SEQ ID NO. 428) hknnedikndnskdikndnskdikndnsk (SEQ ID NO. 429) hknnedikndnskdikndnskdik (SEQ ID NO. 430) hknnedikndnskdikndnsk (SEQ ID NO. 431) hknnedikndnskdik (SEQ ID NO. 432) hknnedik (SEQ ID NO. 433) kkyddlqnkynilnklknsleekneelkkyh (SEQ ID NO. 434) kyddlqnkynilnklknsleekneelkkyh (SEQ ID NO. 435) kynilnklknsleekneelkkyh (SEQ ID NO. 436) klknsleekneelkkyh (SEQ ID NO. 437) knsleekneelkkyh (SEQ ID NO. 438) kneelkkyh (SEQ ID NO. 439) hmgnnqdinenvynikpqefkeeeeedismvntk (SEQ ID NO. 440) k knsnelkrindnffklh (SEQ ID NO. 441) kpclykkckisqclykkckisqvwwcmpvkdtfn (SEQ ID NO. 442) tyernnvlnskienniekiph hinneytnknpkncllykneernydnnikdyins (SEQ ID NO. 443) mnfkk hinneytnknpkncllykneernydnnikdyins (SEQ ID NO. 444) mnfk hinneytnknpkncllyk (SEQ ID NO. 445) knktnqskgvkgeyekkketngh (SEQ ID NO. 446) ktnqskgvkgeyekkketngh (SEQ ID NO. 447) kgvkgeyekkketngh (SEQ ID NO. 448) kgeyekkketngh (SEQ ID NO. 449) ksgmytnegnkscecsykkkssssnkvh (SEQ ID NO. 450) kscecsykkkssssnkvh (SEQ ID NO. 451) kkkssssnkvh (SEQ ID NO. 452) kkssssnkvh (SEQ ID NO. 453) kssssnkvh (SEQ ID NO. 454) himlksgmytnegnkscecsykkkssssnk (SEQ ID NO. 455) himlksgmytnegnkscecsykkk (SEQ ID NO. 456) himlksgmytnegnkscecsykk (SEQ ID NO. 457) himlksgmytnegnkscecsyk (SEQ ID NO. 458) kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 459) iirdyhetlnvhkldh krektqinktkyergdviidnteiqkiiirdyhe (SEQ ID NO. 460) tlnvhkldh ktqinktkyergdviidnteiqkiiirdyhetln (SEQ ID NO. 461) vhkldh kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 462) iirdyhetlnvh kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 463) iirdyh klrkrektqinktkyergdviidnteiqkiiird (SEQ ID NO. 464) yh krektqinktkyergdviidnteiqkiiiidyh (SEQ ID NO. 465) ktqinktkyergdviidnteiqkiiirdyh (SEQ ID NO. 466) kkdkekkkdsnenrkkkqkedkknpndnklkkie (SEQ ID NO. 467) ytnkith kdkekkkdsnenrkkkqkedkknpndnklkkiey (SEQ ID NO. 468) tnkith kekkkdsnenrkkkqkedkknpndnklkkieytn (SEQ ID NO. 469) kith kkkdsnenrkkkqkedkknpndnklkkieytnki (SEQ ID NO. 470) th kkdsnenrkkkqkedkknpndnklkkieytnkit (SEQ ID NO. 471) h kdsnenrkkkqkedkknpndnklkkieytnkith (SEQ ID NO. 472) kkkqkedkknpndnklkkieytnkith (SEQ ID NO. 473) kkqkedkknpndnklkkieytnkith (SEQ ID NO. 474) kqkedkknpndnklkkieytnkith (SEQ ID NO. 475) kedkknpndnklkkieytnkith (SEQ ID NO. 476) kknpndnklkkieytnkith (SEQ ID NO. 477) knpndnklkkieytnkith (SEQ ID NO. 478) klkkieytnkith (SEQ ID NO. 479) kkieytnkith (SEQ ID NO. 480) kieytnkith (SEQ ID NO. 481) hgqikiedvnnenfnneqmknkyndeekmdisks (SEQ ID NO. 482) kslksdflek hgqikiedvnnenfnneqmknkyndeekmdisks (SEQ ID NO. 483) kslk hgqikiedvnnenfnneqmknkyndeekmdisks (SEQ ID NO. 484) k hgqikiedvnnenThneqmknkyndeekmdisk (SEQ ID NO. 485) kkyddlqnkynilnklknsleekneellckyh (SEQ ID NO. 486) kyddlqnkynilnklknsleekneelkkyh (SEQ ID NO. 487) kynilfildknsleekneelkkyh (SEQ ID NO. 488) klknsleekneellckyh (SEQ ID NO. 489) knsleekneellckyh (SEQ ID NO. 490) kneellckyh (SEQ ID NO. 491) hmgnnqdinenvynikpqefkeeeeedismvntk (SEQ ID NO. 492) kcddiqenik ktnlyniynnknddkdnildnenreglylcdvmk (SEQ ID NO. 493) nsnelkrindnffklh knsnelkrindnffklh (SEQ ID NO. 494) krindnffidh (SEQ ID NO. 495) hinneytnknpkncllykneernyndnnikdyin (SEQ ID NO. 496) smnfkk hinneytnknpkncllykneernyndnnikdyin (SEQ ID NO. 497) smnfk hinneytnknpkncllyk (SEQ ID NO. 498) kpclykkckisqvwwcmpvkdtfntyernnvlns (SEQ ID NO. 499) kienniekiph kckisqvwwcmpvkdtfntyernnvlnskienni (SEQ ID NO. 500) ekiph kienniekiph (SEQ ID NO. 501) knktngskgvkgeyekkketngh (SEQ ID NO. 502) ktngskgvkgeyekkketngh (SEQ ID NO. 503) kgvkgeyekkketngh (SEQ ID NO. 504) kgeyekkketngh (SEQ ID NO. 505) ktiekinkskswffeeldeidkplaklrkrektq (SEQ ID NO. 506) inktkyergdviidnteiqkiirdyh kinkskswffeeldeidkplaklrkrektqinkt (SEQ ID NO. 507) kyergdviidnteiqkiirdyh kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 508) irdyh himlksqmytnegnkscecsykkkssssnkvh (SEQ ID NO. 509) klrkrektqinktkyergdviidnteiqkiirdy (SEQ ID NO. 510) h krektqinktkyergdviidnteiqkiirdyh (SEQ ID NO. 511) ktqinktkyergdviidnteiqkiirdyh (SEQ ID NO. 512) kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 513) irdyhtlnvhkldh klrkrektqinktkyergdviidnteiqkiirdy (SEQ ID NO. 514) htlnvhkldh krektqinktkyergdviidnteiqkiirdyhtl (SEQ ID NO. 515) nvhkldh ktqinktkyergdviidnteiqkiirdyhtlnvh (SEQ ID NO. 516) kldh kplaklrkrektqinktkyergdviidnteiqki (SEQ ID NO. 517) irdyhtlnvh klrkrektqinktkyergdviidnteiqkiirdy (SEQ ID NO. 518) htlnvh krektqinktkyergdviidnteiqkiirdyhtl (SEQ ID NO. 519) nvh ktqinktkyergdviidnteiqkiirdyhtlnvh (SEQ ID NO. 520) himlksqmytnegnkscecsykkkssssnkvh (SEQ ID NO. 521) ksqmytnegnkscecsykkkssssnkvh (SEQ ID NO. 522) kscecsykkkssssnkvh (SEQ ID NO. 523) kkkssssnkvh (SEQ ID NO. 524) kkssssnkvh (SEQ ID NO. 525) kssssnkvh (SEQ ID NO. 526) himlksqmytnegnkscecsykkkssssnk (SEQ ID NO. 527) himlksqmytnegnkscecsykkk (SEQ ID NO. 528) himlksqmytnegnkscecsykk (SEQ ID NO. 529) himlksqmylnegnkscecsyk (SEQ ID NO. 530) hnnhniqiykdkrinfmnphkvmyhdnmsknert (SEQ ID NO. 531) ek hnnhniqiykdkrinfmnphkvmyhdnmsk (SEQ ID NO. 532) hnnhniqiykdkrinfmnphk (SEQ ID NO. 533) hkvmyhdnmsknertek (SEQ ID NO. 534) hkvmyhdnmsk (SEQ ID NO. 535)

Synthetic Replikin vaccines, based on Replikins such as the glioma Replikin (SEQ ID NO.: 1) “kagvaflhkk” or the hepatitis C Replikin (SEQ ID NO.: 18) “hyppkpgcivpak”, or HIV Replikins such as (SEQ ID NO.: 5) “kcfncgkegh” or (SEQ ID NO.: 6) “kvylawvpahk” or preferably, an influenza vaccine based on conserved and/or emerging or re-emerging Replikin(s) over a given time period may be used to augment antibody concentration in order to lyse the respective virus infected cells and release virus extracellularly where chemical treatment can then be effective. Similarly, a malaria vaccine, based on Replikins observed in Plasmodium falciparum malaria antigens on the merozoite surface or within the parasitophorous vacuole, for example, can be used to generate cytotoxic antibodies to malaria. Recognin and/or Replikin peptides may be administered to a subject to induce the immune system of the subject to produce anti-Replikin antibodies. Generally, a 0.5 to about 2 mg dosage, preferably a 1 mg dosage of each peptide is administered to the subject to induce an immune response. Subsequent dosages may be administered if desired.

In another embodiment of the invention, isolated Replikin peptides may be used to generate antibodies, which may be used, for example to provide passive immunity in an individual. Passive immunity to- the strain of influenza identified by the method of the invention to be the most likely cause of future influenza infections may be obtained by administering antibodies to Replikin sequences of-the identified strain of influenza virus to patients in need. Similarly, passive immunity to malaria may be obtained by administering antibodies to Plasmodium falciparum Replikin(s).

Various procedures known in the art may be used for the production of antibodies to Replikin sequences. Such antibodies include but are not limited to polyclonal, monoclonal, chimeric, humanized, single chain, Fab fragments and fragments produced by an Fab expression library. Antibodies that are linked to a cytotoxic agent may also be generated. Antibodies may also be administered in combination with an antiviral agent. Furthermore, combinations of antibodies to different Replikins may be administered as an antibody cocktail.

For the production of antibodies various host animals may be immunized by injection with a Replikin peptide or a combination of Replikin peptides, including but not limited to rabbits, mice, rats, and larger mammals. Various adjuvants may be used to enhance the immunological response, depending on the host species, including but not limited to Freund's (complete and incomplete), mineral gels, such as aluminum hydroxide, surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, key limpet hemocyanin, dintrophenol, and potentially useful human adjuvants such as BCG and Corynebacterium parvum.

Monoclonal antibodies to Replikins may be prepared by using any technique that provides for the production of antibody molecules. These include but are not limited to the hybridoma technique originally described by Kohler and Milstein, (Nature, 1975, 256:495-497), the human B-cell hybridoma technique (Kosbor et al., 1983, Immunology Today, 4:72), and the EBV hybridoma technique (Cole et al., Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc., pp. 77-96). In addition, techniques developed for the production of chimeric antibodies (Morrison et al., 1984, Proc. Nat. Acad. Sci USA, 81:6851-6855) or other techniques may be used. Alternatively, techniques described for the production of single chain antibodies (U.S. Pat. No. 4,946,778) can be adapted to produce Replikin-specific single chain antibodies.

Particularly useful antibodies of the invention are those that specifically bind to Replikin sequences contained in peptides and/or polypeptides of influenza virus. For example, antibodies to any of peptides observed to be present in an emerging or re-emerging strain of influenza virus and combinations of such antibodies are useful in the treatment and/or prevention of influenza. Similarly, antibodies to any replikins present on malaria antigens and combinations of such antibodies are useful in the prevention and treatment of malaria.

Antibody fragments which contain binding sites for a Replikin may be generated by known techniques. For example, such fragments include but are not limited to F(ab′)₂ fragments which can be produced by pepsin digestion of the antibody molecules and the Fab fragments that can be generated by reducing the disulfide bridges of the F(ab′)₂ fragments. Alternatively, Fab expression libraries can be generated (Huse et al., 1989, Science, 246:1275-1281) to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity.

The fact that antimalignin antibody is increased in concentration in human malignancy regardless of cancer cell type (FIG. 5), and that this antibody binds to malignant cells regardless of cell type now may be explained by the presence of the Replikin structures herein found to be present in most malignancies (FIG. 1 and Table 2). Population studies have shown that antimalignin antibody increases in concentration in healthy adults with age, and more so in high-risk families, as the frequency of cancer increases. An additional two-fold or greater antibody increase which occurs in early malignancy has been independently confirmed with a sensitivity of 97% in breast cancers 1-10 mm in size. Shown to localize preferentially in malignant cells in vivo, histochemically the antibody does not bind to normal cells but selectively binds to (FIG. 4 a,b) and is highly cytotoxic to transformed cells in vitro (FIG. 4 c-f). Since in these examples the same antibody is bound by several cell types, that is, brain glioma, hematopoietic cells (leukemia), and small cell carcinoma of lung, malignant Replikin class unity is again demonstrated.

Antimalignin does not increase with benign proliferation, but specifically increases only with malignant transformation and replication in breast in vivo and returns from elevated to normal values upon elimination of malignant cells (FIG. 5). Antimalignin antibody concentration has been shown to relate quantitatively to the survival of cancer patients, that is, the more antibody, the longer the survival. Taken together, these results suggest that anti-Replikin antibodies may be a part of a mechanism of control of cell transformation and replication. Augmentation of this immune response may be useful in the control of replication, either actively with synthetic Replikins as vaccines, or passively by the administration of anti-Replikin antibodies, or by the introduction of non-immune based organic agents, such as for example, carbohydrates, lipids and the like, which are similarly designed to target the Replikin specifically. For organisms such as diatom plankton, foot and mouth disease virus, tomato leaf curl gemini virus, hepatitis B and C, HIV, influenza virus and malignant cells, identified constituent Replikins are useful as vaccines, and also may be usefully targeted for diagnostic purposes. Blood collected for transfusions, for example, may be screened for contamination of organisms, such as HIV, by screening for the presence of Replikins shown to be specific for the contamination organism. Also, screening for Replikin structures specific for a particular pathological organism, e.g., anthrax, leads to diagnostic detection of the organism in body tissue or in the environment.

The Replikin sequence structure is associated with the function of replication. Thus, whether the Replikins of this invention are used for targeting sequences that contain Replikins for the purpose of diagnostic identification, promoting replication, or inhibiting or attacking replication, for example, the structure-function relationship of the Replikin is fundamental. Thus, while the structure of the Replikin may be a part of a larger protein sequence, which may have been previously identified, it is preferable to utilize only the specific Replikin structure when seeking to induce antibodies that will recognize and attach to the Replikin fragment and thereby cause destruction of the cell. Even though the larger protein sequence may be known in the art as having a “replication associated function,” vaccines using the larger protein often have failed or proven ineffective, even though they contain one or more Replikin sequences.

Although the present inventors do not wish to be held to a single theory, the studies herein suggest that the prior art vaccines are ineffective because they are based on the use of the larger protein sequence. The larger protein sequence invariably has one or more epitopes (independent antigenic sequences that can induce specific antibody formation); Replikin structures usually comprise one of these potential epitopes. The presence of other epitopes within the larger protein may interfere with adequate formation of antibodies to the Replikin, by “flooding” the immune system with irrelevant antigenic stimuli which may preempt the. Replikin antigens, See, e.g., Webster, R. G., J. Immunol., 97(2):177-183 (1966); and Webster et al., J. Infect. Dis., 134:48-58, 1976; Klenerman et al, Nature 394:421-422 (1998) for a discussion of the well-known phenomenon “original antigenic sin”). The formation of an antibody to a non-Replikin epitope may allow binding to the cell, but not necessarily lead to cell destruction. The presence of structural “decoys” on the C-termini of malaria proteins is another aspect of this ability of other epitopes to interfere with binding of effective anti-Replikin antibodies, since the- decoy epitopes have many lysine residues,.but no histidine residues. Thus, decoy epitopes may bind anti-Replikin antibodies, but keep the antibodies away from histidine-bound respiratory enzymes.

It is well known in the art that in the course of antibody production against a “foreign” protein, the protein is first hydrolyzed into smaller fragments. Usually fragments containing from about six to ten amino acids are selected for antibody formation. Thus, if hydrolysis of a protein does not result in Replikin-containing fragments, anti-Replikin antibodies will not be produced. In this-regard, it is interesting that Replikins contain lysine residues located six to ten amino acids apart, since lysine residues are known to bind to membranes.

Furthermore, Replikin sequences contain at least one histidine residue. Histidine is frequently involved in binding to redox centers. Thus, an antibody that specifically recognizes a Replikin sequence has a better chance of inactivating or destroying the cell in which the Replikin is located, as seen with anti-malignin antibody, which is perhaps the most cytotoxic antibody yet described, being active at picograms per cell.

One of the reasons that vaccines directed towards a particular protein antigen of a disease causing agent have not been filly effective in providing protection against the disease (such as foot and mouth vaccine which has been developed against the VP1 protein or large segments of the VP1 protein) is that antibody to the Replikins have not been produced. That is, either epitopes other than Replikins present in the larger protein fragments may interfere according to-the phenomenon of “original antigenic sin”, and/or because the hydrolysis of larger protein sequences into smaller sequences for processing to produce antibodies results in loss of integrity of any Replikin structure that is present, e.g., the Replikin is cut in two and/or the histidine residue is lost in the hydrolytic processing. The present studies suggest that for an effective vaccine to be produced, the Replikin sequences, and no other epitope, should be used as the vaccine. For example, a vaccine of the invention can be generated using any one of the Replikin peptides identified by the three point recognition system. Particularly preferred peptides for an influenza vaccine include peptides that have been demonstrated to be conserved over a period of one or more years, preferably about three years or more, and/or which are present in a strain of influenza virus shown to have the highest increase in concentration of Replikins relative to Replikin concentration in other influenza virus strains, e.g., an emerging strain. The increase in Replikin concentration preferably occurs over a period of at least about six months to one year, preferably at least about two years or more, and most preferably about three years or more. Among the preferred Replikin peptides for use in an influenza virus vaccine are those replikins observed to “re-emerge” after an absence from the hemagglutinin amino acid sequence for one or more years.

The Replikin peptides of the invention, alone or in various combinations are administered to a subject, preferably by i.v. or intramuscular injection, in order to stimulate the immune system of the subject to produce antibodies to the peptide. Generally the dosage of peptides is in the range of from about 0.1 μg to about 10 mg, preferably about 10 μg to about 1 mg, and most preferably about 50 μg to about 500 ug. The skilled practitioner can readily determine the dosage and number of dosages needed to produce an effective immune response.

Replikin DNA or RNA may have a number of uses for the diagnosis of diseases resulting from infection with a virus, bacterium or other Replikin encoding agent. For example, Replikin nucleotide sequences may be used in hybridization assays of biopsied tissue or blood, e.g., Southern or Northern analysis, including in situ hybridization assays, to diagnose the presence of a particular organism.

Also within the scope of the invention are oligoribonucleotide sequences, that include antisense RNA and DNA molecules and ribozymes that function to inhibit the translation of Replikin- or recognin-containing mRNA. Both antisense RNA and DNA molecules and ribozymes may be prepared by any method known in the art. The antisense molecules can be incorporated into a wide variety of vectors for delivery to a subject. The skilled practitioner can readily determine the best route of delivery, although generally i.v. or i.m. delivery is routine. The dosage amount is also readily ascertainable.

Particularly preferred antisense nucleic acid molecules are those that are complementary to a Replikin sequence contained in a mRNA encoding an influenza virus polypeptide, wherein the Replikin sequence comprises from 7 to about 50 amino acids including (1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues. More preferred are antisense nucleic acid molecules that are complementary to a Replikin present in the coding strand of the gene or to the mRNA encoding the influenza virus hemagglutinin protein, wherein the antisense nucleic acid molecule is complementary to a nucleotide sequence encoding a Replikin that has been demonstrated to be conserved over a period of six months to one or more years and/or which are present in a strain of influenza virus shown to have an increase in concentration of Replikins relative to Replikin concentration in other influenza virus strains. The increase in Replikin concentration preferably occurs over a period of at least six months, preferably about one year, most preferably about two or three years or more.

In another embodiment of the invention, immune serum containing antibodies to one or more Replikins obtained from an individual exposed to one or more Replikins may be used to induce passive immunity in another individual or animal. Immune serum may be administered via i.v. to a subject in need of treatment. Passive immunity also can be achieved by injecting a recipient with preformed antibodies to one or more Replikins. Passive immunization may be used to provide immediate protection to individuals who have been exposed to an infectious organism. Administration of immune serum or preformed antibodies is routine and the skilled practitioner can readily ascertain the amount of serum or antibodies needed to achieve the desired effect.

In another aspect of the invention, Replikin structures are used to increase the replication of of organisms. The present invention demonstrates that in influenza virus, for example, increased replication associated with epidemics is associated with increased concentration of Replikins. The increase is due to 1) the reappearance of particular replikin structures, which were present in previous years, but which then disappeared for one or more years; and/or 2) by the appearance of new replikin compositions. In addition, in malaria Replikins, repetition of the same Replikin in a single protein occurs. Thus, the present invention provides methods and compositions for increasing the replication of organisms. For example, the production of crops which are critical to feeding large populations throughout the world, such as rice, for example, can be improved by increasing the concentration (number of Replikins/100 amino acid residues) of any particular strain of the food crop.

As an example, in the Oryza sativa strain of rice, catalase isolated from immature seeds was observed to contain three different Replikins within the 491 amino acid sequence of the protein. Thus, by using recombinant gene cloning techniques well known in the art, the concentration of Replikin structures in an organism, such as a food crop plant, can be increased, which will promote increased replication of the organism.

The present invention also provides methods for identifying Replikin sequences in an amino acid or nucleic acid sequence. Visual scanning of over four thousand sequences was performed in developing the present 3-point-recognition methods. However, data banks comprising nucleotide and/or amino acid sequences can also be scanned by computer for the presence of sequences meeting the 3 point recognition requirements.

The three point recognition method may also be modified to identify other useful compounds of covalently linked organic molecules, including other covalently linked amino acids, nucleotides, carbohydrates, lipids or combinations thereof. In this embodiment of the invention a sequence is screened for subsequences containing three or more desired structural characteristics. In the case of screening compounds composed of covalently linked amino acids, lipids or carbohydrates the subsequence of 7 to about 50 covalently linked units should contain (1) at least one first amino acid, carbohydrate or lipid residue located seven to ten residues from a second of the first amino acid, carbohydrate or lipid residue; (2) encoding at least one second amino acid, lipid or carbohydrate residue; and (3) at least 6% of the first amino acid, carbohydrate or lipid residue. In the case of screening nucleotide sequences, the subsequence of about 21 to about 150 nucleotides should contain (1) at least one codon encoding a first amino acid located within eighteen to thirty nucleotides from a second codon encoding the first amino acid residue; (2) at least one second amino acid residue; and (3) encodes at least 6% of said first amino acid residue.

According to another embodiment of the invention, the methods described herein may be performed by a computer. FIG. 6 is a block diagram of a computer available for use with the foregoing embodiments of the present invention. The computer may include a processor, an input/output device and a memory storing executable program instructions representing the 3-point-recognition methods of the foregoing embodiments. The memory may include a static memory, volatile memory and/or a nonvolatile memory. The static memory conventionally may be a read only memory (“ROM”) provided on a magnetic, or an electrical or optical storage medium. The volatile memory conventionally may be a random access memory (“RAM”) and may be integrated as a cache within the processor or provided externally from the processor as a separate integrated circuit. The non-volatile memory may be an electrical, magnetic or optical storage medium.

From a proteomic point of view the construction of a “3-point-recognition” template based on the new glioma peptide sequence led directly to identification of a biology-wide class of proteins having related structures and functions. The operation of the 3-point-recognition method resembles identification by the use of a “keyword”search; but instead of using the exact spelling of the keyword “kagvaflhkk” (SEQ ID NO.: 1) as in a typical sequence homology search, or in the nucleotide specification of an amino acid, an abstraction of the keyword delimited by the “3-point-recognition” parameters is used. This delimited abstraction, although derived from a single relatively short amino acid sequence leads to identification of a class of proteins with structures that are defined by the same specifications. That particular functions, in this case transformation and replication, in addition to structures, turns out also to be shared by members of the exposed class suggests that these structures and functions are related. Thus, from this newly identified short peptide sequence, a molecular recognition ‘language’ has been formulated, which previously has not been described. Further, the sharing of immunological specificity by diverse members of the class, as here demonstrated for the cancer Replikins, suggests that B cells and their product antibodies recognize Replikins by means of a similar recognition language. Since “3-point-recognition” is a proteomic method that specifies a particular class of proteins, using three or more different recognition points for other peptides similarly should provide useful information concerning other proteins classes. Further, the “3-point-recognition” method is applicable to other recognins, for example to the TOLL ‘innate’ recognition of lipopolyssacharides of organisms.

Several embodiments of the present invention are specifically illustrated and described herein. However, it will be appreciated that modifications and variations of the present invention are encompassed by the above teachings and within the purview of the appended claims without departing from the spirit and intended scope of the invention.

EXAMPLE 1

Process for Extraction, Isolation and Identification of Replikins and the Use of Replikins to Target, Label or Destroy Replikin-Containing Organisms

a) Algae

The following algae were collected from Bermuda water sites and either extracted on the same day or frozen at −20 degrees C. and extracted the next day. The algae were homogenized in a cold room (at 0 to 5 degrees C.) in 1 gram aliquots in neutral buffer, for example 100 cc. of 0.005M phosphate buffer solution, pH 7 (“phosphate buffer”) for 15 minutes in a Waring blender, centrifuged at 3000 rpm, and the supernatant concentrated by perevaporation and dialyzed against phosphate buffer in the cold to produce a volume of approximately 15 ml. The volume of this extract solution was noted and an aliquot taken for protein analysis, and the remainder was fractionated to obtain the protein fraction having a pK range between 1 and 4. The preferred method of fractionation is chromatography as follows:

The extract solution is fractionated in the cold room (4 degrees C.) on a DtAE cellulose (Cellex-D) column 2.5×11.0 cm, which has been equilibrated with 0.005M phosphate buffer. Stepwise eluting solvent changes are made with the following solutions:

Solution 1—4.04 g. NaH2P04 and 0.5 g NaH2P04 are dissolved in 15 litres of distilled water (0.005 molar, pH 7);

Solution 2—8.57 g. NaH2P04 is dissolved in 2,480 ml. of distilled water;

Solution 3—17.1 g. of NaH2P04 is dissolved in 2480 ml of distilled water (0.05 molar, pH 4.7);

Solution 4—59.65 g. of NaH2P04 is dissolved in 2470 ml distilled water (0.175 molar);

-   -   Solution 5—101.6 g. of NaH2P04 is dissolved in 2455 ml distilled         water (pH 4.3);     -   Solution 6—340.2 g. of NaH2P04 is dissolved in 2465 of distilled         water (1.0 molar, pX-i 4.1);     -   Solution 7—283.63 g. of 80% phosphoric acid (H3P04) is made up         in 2460 ml of distilled water (1.0 molar, pH 1.0).

The extract solution, in 6 to 10 ml volume, is passed onto the column and overlayed with Solution 1, and a reservoir of 300 ml of Solution 1 is attached and allowed to drip by gravity onto the column. Three ml aliquots of eluant are collected and analyzed for protein content at OD 280 until all of the protein to be removed with Solution 1 has been removed from the column. Solution 2 is then applied to the column, followed in succession by Solutions 3, 4, 5, 6 aid 7 until all of the protein which can, be removed with each Solution is removed from the column. The eluates from Solution 7 are combined, dialyzed against phosphate buffer, the protein content determined of both dialys and and dialyzate, and both analyzed by gel electrophoresis. One or two bands of peptide or protein of molecular weight between 3,000 and 25,000 Daltons are obtained in Solution 7. For example the algae Caulerpa mexicana, Laurencia obtura, Cladophexa prolifera, Sargassum natans, Caulerpa verticillata, Halimeda tuna, and Penicillos capitatus, after extraction and treatment as above, all demonstrated in Solution 7 eluates sharp peptide bands in this molecular weight region with no contaminants. These Solution 7 proteins or their eluted bands are hydrolyzed, and the amino acid composition determined. The peptides so obtained, which have a lysine composition of 6% or greater are Replikin precursors. These Replikin peptide precursors are then determined for amino acid sequence and the replikins are determined by hydrolysis and mass spectrometry as detailed in U.S. Pat. No. 6,242,578 B1. Those which fulfill the criteria defined by the “3-point-recognition” method are identified as Replikins. This procedure can also be applied to obtain yeast, bacterial and any plant Replikins.

b) Virus

Using the same extraction and- column chromatography separation methods as above in a) for algae, Replikens in virus-infected cells are isolated and identified.

c) Tumor Cells in vivo and in vitro Tissue Culture

Using the same extraction and column chromatography separation methods as above in a) for algae, Replikins in tumor cells are isolated and identified. For example, Replikin precursors of Astrocytin isolated from malignant brain tumors, Malignin (Aglyco lOB) isolated from glioblastoma tumor cells in tissue cuOlture, MCF7 mammary- carcinoma cells in tissue culture, and P₃J Lymphoma cells in tissue culture each treated as above in a) yielded Replikin precursors with lysine content of 9.1%, 6.7%, 6.7%, and 6.5% respectively. Hydrolysis and mass spectrometry of Aglyco lOB as described in Example 10 U.S. Pat. No. 6,242,578 B1 produced the amino acid sequence, ykagvaflhkkndiide the 16-mer Replikin.

EXAMPLE 2

As an example of diagnostic use of Replikins: Aglyco lOB or the 16-mer Repliken may be used as antigen to capture and quantify the amount of its corresponding antibody present in serum for diagnostic purposes are as shown in FIGS. 2,3,4 and 7 of U.S. Pat. No. 6,242,578 B1.

As an example of the production of agents to attach to Replikins for labeling, nutritional or destructive purposes: Injection of the 16-mer Replikin into rabbits to produce the specific antibody to the 16-mer Replikin is shown in Example 6 and FIGS. 9A and 9B of U.S. Pat. No. 6,242,578 B1.

As an example of the use of agents to label Replikins: The use of antibodies to the 16-mer Replikin to label specific cells which contain this Replikin is shown in FIG. 5 and Example 6 of U.S. 6,242,578 B1.

As an example of the use of agents to destroy Replikins: The use of antibodies to the 16-mer Replikin to inhibit or destroy specific cells which contain this Replikin is shown in FIG. 6 of U.S. Pat. No. 6,242,578 B1.

EXAMPLE 3

Analysis of sequence data of isolates of influenza virus hemagglutinin protein or neuraminidase protein for the presence and concentration of Replikins is carried out by visual scanning of sequences or through use of a computer program based on the 3-point recognition system described herein. Isolates of influenza virus are obtained and the amino acid sequence of the influenza hemagglutinin and/or neuraminidase protein is obtained by any art known method, such as by sequencing the hemagglutinin or neuraminidase gene and deriving the protein sequence therefrom. Sequences are scanned for the presence of new Replikins, conservation of Replikins over time and concentration of Replikins in each isolate. Comparison of the Replikin sequences and concentrations to the amino acid sequences obtained from isolates at an earlier time, such as about six months to about three years earlier, provides data that are used to predict the emergence of strains that are most likely to be the cause of influenza in upcoming flu seasons, and that form the basis for seasonal influenza peptide vaccines or nucleic acid based vaccines. Observation of an increase in concentration, particularly a stepwise increase in concentration of Replikins in a given strain of influenza virus for a period of about six months to about three years or more is a predictor of emergence of the strain as a likely cause of influenza epidemic or pandemic in the future.

Peptide vaccines or nucleic acid-based vaccines based on the Replikins observed in the emerging strain are generated. An emerging strain is identified as the strain of influenza virus-having the highest increase in concentration of replikin sequences within the hemagglutinin and/or neuraminidase sequence during the time period. Preferably, the peptide or nucleic acid vaccine is based on or includes any Replikin sequences that are observed to be conserved in the emerging strain. Conserved replikins are preferably those Replikin sequences which are present in the hemagglutinin or neuraminidase protein sequence for about two years and preferably longer. The vaccines may include any combination of Replikin sequences identified in the emerging strain.

For vaccine production, the Replikin peptide or peptides identified as useful for an effective vaccine are synthesized by any method, including chemical synthesis and molecular biology techniques, including cloning, expression in a host cell and purification therefrom. The peptides are preferably admixed with a pharmaceutically acceptable carrier in an amount determined to induce a therapeutic antibody reaction thereto. Generally, the dosage is about 0.1 μg to about 10 mg.

The influenza vaccine is preferably administered to a patient in need thereof prior to the onset of “flu season.” Influenza flu season generally occurs in late October and lasts through late April. However, the vaccine may be administered at any time during the year. Preferably, the influenza vaccine is administered once yearly, and is based on Replikin sequences observed to be present, and preferably conserved in the emerging strain of influenza virus. Another preferred Replikin for inclusion in an influenza vaccine is a Replikin demonstarated to have re-emerged in a strain of influenza after an absence of one or more years.

EXAMPLE 4

Analysis of sequence data of isolates of Plasmodium falciparum antigens for the presence and concentration of Replikins is carried out by visual scanning of sequences or through use of a computer program based on the 3-point recognition system described herein. Isolates of Plasmodium falciparum are obtained and the amino acid sequence of the protein is obtained by any art known method, such as by sequencing the gene and deriving the protein sequence therefrom. Sequences are scanned for the presence of Replikins, conservation of Replikins over time and concentration of Replikins in each isolate. This information provides data that are used to form the basis for anti-malarial peptide vaccines or nucleic acid based vaccines.

Peptide vaccines or nucleic acid-based vaccines based on the Replikins observed in the malaria causing organism are generated. Preferably, the peptide or nucleic acid vaccine is based on or includes any Replikin sequences that are observed to be present on a surface antigen of the organism. The vaccines may include any combination of Replikin sequences identified in the malaria causing strain.

For vaccine production, the Replikin-peptide or peptides identified as useful for an effective vaccine are synthesized by any method, including chemical synthesis and molecular biology techniques, including cloning, expression in a host cell and purification therefrom. The peptides are preferably admixed with a pharmaceutically acceptable carrier in an amount determined to induce a therapeutic antibody reaction thereto. Generally, the dosage is about 0.1 μg to about 10 mg.

Then malaria vaccine is preferably administered to a patient in need thereof at any time during the year, and particularly prior to travel to a tropical environment. 

1-35. (canceled)
 36. An isolated Plasmodium falciparum peptide comprising (1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.
 37. The peptide of claim 36 comprising overlapping replikins.
 38. An antibody that specifically binds to a Plasmodium falciparum peptide sequence having (1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.
 39. An antibody cocktail comprising a plurality of antibodies, wherein each of the plurality of antibodies specifically binds to a Plasmodium falciparum peptide sequence having (1) at least one lysine residue located six to ten residues from a second lysine residue; (2) at least one histidine residue; and (3) at least 6% lysine residues.
 40. A composition comprising the antibody of claim 38 or antibody cocktail of claim 39 and a pharmaceutical composition.
 41. A method of stimulating the immune system of a subject to produce antibodies to Plasmodium falciparum comprising administering to the subject an effective amount of at least one Plasmodium falciparum Replikin and a pharmaceutically acceptable carrier.
 42. The method of claim 41 wherein the replikin is located on the merozoite surface or within the parasitophorous vacuole of the Plasmodium falciparum. 43-48. (canceled) 